• 3QNQ Assumed Biological Molecule
    3QNQ
    Crystal structure of the transporter ChbC, the IIC component from the N,N'-diacetylchitobiose-specific phosphotransferase system
  • 3ME1 Assumed Biological Molecule
    3ME1
    Crystal Structure of the Desulfovibro vulgaris Urea Transporter in the P3(1) Space Group at 3.86
  • 3PJZ Assumed Biological Molecule
    3PJZ
    Crystal Structure of the Potassium Transporter TrkH from Vibrio parahaemolyticus
  • 3M6E Assumed Biological Molecule
    3M6E
    F80A mutant of the Urea Transporter from Desulfovibrio Vulgaris
  • 3M70 Assumed Biological Molecule
    3M70
    Crystal Structure of TehB from Haemophilus influenzae
  • 3M71 Assumed Biological Molecule
    3M71
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M72 Assumed Biological Molecule
    3M72
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M73 Assumed Biological Molecule
    3M73
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M74 Assumed Biological Molecule
    3M74
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M75 Assumed Biological Molecule
    3M75
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M76 Assumed Biological Molecule
    3M76
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M77 Assumed Biological Molecule
    3M77
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M78 Assumed Biological Molecule
    3M78
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M7B Assumed Biological Molecule
    3M7B
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M7C Assumed Biological Molecule
    3M7C
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M7E Assumed Biological Molecule
    3M7E
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3M7L Assumed Biological Molecule
    3M7L
    Crystal Structure of Plant SLAC1 homolog TehA
  • 3LLQ Assumed Biological Molecule
    3LLQ
    Aquaporin structure from plant pathogen Agrobacterium Tumerfaciens
  • 3KLY Assumed Biological Molecule
    3KLY
    Pentameric formate channel
  • 3KLZ Assumed Biological Molecule
    3KLZ
    Pentameric formate channel with formate bound
  • 3K3F Assumed Biological Molecule
    3K3F
    Crystal Structure of the Urea Transporter from Desulfovibrio Vulgaris
  • 3K3G Assumed Biological Molecule
    3K3G
    Crystal Structure of the Urea Transporter from Desulfovibrio Vulgaris Bound to 1,3-dimethylurea
  • 3GI8 Assumed Biological Molecule
    3GI8
    Crystal Structure of ApcT K158A Transporter Bound to 7F11 Monoclonal Fab Fragment
  • 3GI9 Assumed Biological Molecule
    3GI9
    Crystal Structure of ApcT Transporter Bound to 7F11 Monoclonal Fab Fragment
  • 3GIA Assumed Biological Molecule
    3GIA
    Crystal Structure of ApcT Transporter
  • 2K2B Asymmetric Unit
    2K2B
    Sparse-constraint solution NMR structure of micelle-solublized cytosolic amino terminal domain of C. elegans mechanosensory ion channel subunit MEC-4. New York Consortium on Membrane Protein Structure (NYCOMPS) (CASP TARGET)
  • 2QJU Asymmetric Unit
    2QJU
    Crystal Structure of an NSS Homolog with Bound Antidepressant

MISSION

The NYCOMPS consortium aims to accelerate the acquisition of structural information about membrane proteins by applying a structural genomics approach informed by the collective experience of a team of expert investigators. We have established the New York Consortium on Membrane Protein Structure (NYCOMPS) to work together toward this objective. Our pipeline for structure determination selects targets through a bioinformatics analysis of all known sequences, moves on to recombinant cloning, protein expression and protein purification at moderately high throughput, and then completes structures by x-ray crystallography. Our Protein Production Facility at the New York Structural Biology Center (NYSBC) handles targets through purification at a mid-scale level; and successful candidates are distributed to participant laboratories for scale-up and crystallization. Functional analysis of structures is performed both by computations and through routine experimental biochemistry. Targets are identified through nominations from the biological community and from NYCOMPS biological themes. Our biological themes include the overarching aspiration to explore the complete space of sequence-structure relationships for membrane proteins, with a particular focus on human proteins, and a second theme concerns membrane proteins associated with diabetes and related metabolic disorders.


Become a NYCOMPS adjunct member!
Structural biology princliple investigators in the North East can apply to become a NYCOMPS adjunct member. You can choose to have your protein of interest passed through the NYCOMPS pipeline. The PSI policies and mechanism to do this are listed here. Or take verified membrane proteins expressing clones to work up in your own lab. Contact us for details!

 

NYCOMPS annual meeting to be held on the 18th November 2011 at NYSBC.