Structure and specificity of L-D-Transpeptidase from Mycobacterium tuberculosis and antibiotic resistance: Calcium binding promotes dimer formation
Gokulan, K., Khare, S., Cerniglia, C.E., Foley, S.L., Varughese, K.I.To be published.
Experimental Data Snapshot
wwPDB Validation 3D Report Full Report
Entity ID: 1 | |||||
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Molecule | Chains | Sequence Length | Organism | Details | Image |
L,d-transpeptidase LdtB | 352 | Mycobacterium tuberculosis H37Rv | Mutation(s): 0 Gene Names: ldtB, Rv2518c, RVBD_2518c EC: 2.3.2 | ![]() | |
UniProt | |||||
Find proteins for I6Y9J2 (Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv)) Explore I6Y9J2 Go to UniProtKB: I6Y9J2 | |||||
Entity Groups | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
UniProt Group | I6Y9J2 | ||||
Sequence AnnotationsExpand | |||||
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Ligands 1 Unique | |||||
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ID | Chains | Name / Formula / InChI Key | 2D Diagram | 3D Interactions | |
CA Query on CA | C [auth A] | CALCIUM ION Ca BHPQYMZQTOCNFJ-UHFFFAOYSA-N |
Length ( Å ) | Angle ( ˚ ) |
---|---|
a = 113.758 | α = 90 |
b = 88.132 | β = 90.02 |
c = 90.512 | γ = 90 |
Software Name | Purpose |
---|---|
HKL-2000 | data collection |
MLPHARE | phasing |
REFMAC | refinement |
HKL-2000 | data reduction |
HKL-2000 | data scaling |