GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlD in Salinicoccus carnicancri Crm

Align mannitol-1-phosphate 5-dehydrogenase (EC 1.1.1.17) (characterized)
to candidate WP_017549670.1 C792_RS0111860 mannitol-1-phosphate 5-dehydrogenase

Query= metacyc::MONOMER-13098
         (382 letters)



>NCBI__GCF_000330705.1:WP_017549670.1
          Length = 369

 Score =  278 bits (710), Expect = 2e-79
 Identities = 152/363 (41%), Positives = 222/363 (61%), Gaps = 7/363 (1%)

Query: 3   KAVHFGAGNIGRGFIGQILFENGFAIDFVDVNDKIINALNERHSYDIEIAEDGKRHITVS 62
           KA+HFGAGNIGRGFIG+IL +NG+ + F DV+ +II+ALN+ H Y + IAE+      ++
Sbjct: 2   KAIHFGAGNIGRGFIGKILHDNGYEVTFADVSKEIIDALNKEHGYTVHIAEENGASYDIT 61

Query: 63  NVAGINNKENPQAVIDAVAETELITTAIGPNILPFIAQLIAKGIEKRRESQNQTPLDIIA 122
            V GIN  ENP  +  A+ E ++ITTA+G N+LP I + IA  + +R E  +  PL+IIA
Sbjct: 62  GVNGINTAENPGKLKQAILEADIITTAVGVNVLPIIGKSIAPHLPRRLE--DPRPLNIIA 119

Query: 123 CENMIGGSAFLWQEVQKYLSADGLAFAKDYIGFPNAAVDRIVPAQVHEDPLFVVVEPFSE 182
           CEN +  +  L + +   +   G+  A + IGFPN+AVDRIVP Q +E  L V VEPF E
Sbjct: 120 CENAVMATDTLKEAI---IEETGVLAASN-IGFPNSAVDRIVPVQKNERILDVKVEPFYE 175

Query: 183 WVVETAAMKNPDLKLSSVHYEENLEPFIERKLFSVNSGHATTAYTGAYFGAKTVLEALKD 242
           WV+E    KN + +L    Y   L P+IERKLF+VN+GHA  AY G   G  TV EA+ D
Sbjct: 176 WVIEETEWKN-NKRLDGPVYVRELMPYIERKLFTVNTGHAAIAYYGRTLGYDTVYEAMTD 234

Query: 243 QQVKEQVKAVLGEIRQLLMAKWQFKENDLKVYHDIIISRFENPYIVDDVTRVARTPIRKL 302
            +V+  +  VL E  + + + + F   +  +Y + I  RF NP++ DD+ RV R  +RKL
Sbjct: 235 SKVQNFLSDVLSETLEYITSVYGFTAKEQNIYIEKITERFTNPHLSDDLNRVGRGIMRKL 294

Query: 303 GYDERFIRPIRELKDRGLSYEYLLQTVAYVFHYKDSNDEQSVQLKLLLQEKSLKAVVKEV 362
           G ++R I+P+  L + G S+  L + V Y   + +  D + V++  ++ EK L   + E 
Sbjct: 295 GPNDRIIKPLVHLHNEGKSHRALSELVLYAVKFDNEEDPEQVEMNEIIAEKGLLYFLMEY 354

Query: 363 TGL 365
           +GL
Sbjct: 355 SGL 357


Lambda     K      H
   0.318    0.136    0.384 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 387
Number of extensions: 16
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 382
Length of database: 369
Length adjustment: 30
Effective length of query: 352
Effective length of database: 339
Effective search space:   119328
Effective search space used:   119328
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory