GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Marinomonas arctica 328

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_111608757.1 DK187_RS18225 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_003259225.1:WP_111608757.1
          Length = 366

 Score =  217 bits (553), Expect = 3e-61
 Identities = 129/365 (35%), Positives = 211/365 (57%), Gaps = 28/365 (7%)

Query: 4   IIVKNVSKVFKKGKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTGELY 63
           I +KN++K +    V  LD++N++IE+GE    LGPSG GK+T +R+IAGL+  + G + 
Sbjct: 5   ISIKNITKRYDS--VTVLDDINLHIEDGEFVVFLGPSGCGKSTLLRMIAGLESITEGSIE 62

Query: 64  FDDRLVASNGKLIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKRVEE 123
             D+ + +     +P   R + MVFQ++ALYP++T  +N++F L N+ ++++EI +RV +
Sbjct: 63  IGDKRIDT-----LPSGQRGVAMVFQSYALYPHMTTRQNMSFGLENVNVAQDEIDRRVND 117

Query: 124 VAKILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSARALV 183
            AKIL+I H+L+  P  LSGGQ+QRVA+ RA+VK+P   L DEP SNLDA +R   R  +
Sbjct: 118 AAKILEIDHLLDRKPGRLSGGQRQRVAIGRAIVKEPKAFLFDEPLSNLDAALRGRTRLEL 177

Query: 184 KEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASLIGE 243
            ++  RLG T++ V+HD  +   +ADR+ ++ K K+ Q+G P ++Y +PVS  VA  +G 
Sbjct: 178 AQLHQRLGSTMIFVTHDQVEAMTLADRIVIMHKQKIEQIGTPMEIYQHPVSRFVAEFVGS 237

Query: 244 -------INELEG-------KVTNEGVVIGSLRFPVSVSSDRAIIGIRPEDVKLSKDVIK 289
                  IN +E        +V+  G V+ ++  P   ++  A+IGIR ED  +     +
Sbjct: 238 PPMSMLPINHIENTVDGVTVEVSGAGKVVTAITLPQDFNAKDAVIGIRAEDTAIVSP--Q 295

Query: 290 DDSWILVGKGKVKVIGYQGGLFRITITPLDSEEEIFTYSDH-PIHSGEEVLVYVRKDKIK 348
           ++   L     +KV+   G    +  T +D  E I   +    + +GE V V +      
Sbjct: 296 EEGLDLT----IKVVERLGDRTLLYGTLVDGTELIAEDTGRSKVKAGETVRVSISPHAAH 351

Query: 349 VFEKN 353
           +F+ N
Sbjct: 352 IFDGN 356


Lambda     K      H
   0.319    0.139    0.390 

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: 298
Number of extensions: 18
Number of successful extensions: 3
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: 353
Length of database: 366
Length adjustment: 29
Effective length of query: 324
Effective length of database: 337
Effective search space:   109188
Effective search space used:   109188
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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