GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Desulfovibrio vulgaris Hildenborough

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate 206137 DVU0712 amino acid ABC transporter, periplasmic-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>MicrobesOnline__882:206137
          Length = 376

 Score =  204 bits (518), Expect = 4e-57
 Identities = 124/355 (34%), Positives = 191/355 (53%), Gaps = 12/355 (3%)

Query: 11  VAATAMTASVAKADIAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGVLGQKLKLEV 70
           +AATA  A      + V    P+TG++A+ G+ M+  +E    ++N AGG+ G K++L V
Sbjct: 18  MAATAFAAG----PVRVGLMCPLTGKWASEGQDMRNIVELLAEEVNKAGGINGNKVELIV 73

Query: 71  GDDACDPKQAVAVANQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISPASTNPKLTE 130
            DD  DP+ A   A +L+ +GV  V G + S  +  +  +Y E G+ QI+  STN +LTE
Sbjct: 74  EDDGGDPRTAALAAQKLSTSGVTAVIGTYGSAVTEASQNIYDEAGIAQIATGSTNVRLTE 133

Query: 131 QNLKNVFRVCGRDDQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQKALNAGGQK 190
           + LK   R C RDD+QG++A K +++N   K VA+LHD S+Y KGLADET+  L+  G K
Sbjct: 134 KGLKLFLRTCPRDDEQGRVAAK-VIKNKGYKAVALLHDNSSYAKGLADETKALLDKDGTK 192

Query: 191 EKIYEAYTAGEKDYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLNAPIVSGDAL 250
              Y+A T GE+DY+A+++KLK    D+++  GY+ E G+L RQ  +   N P++ GDA 
Sbjct: 193 IVFYDALTPGERDYTAILTKLKAANPDIIFFTGYYPEVGMLLRQKMEMKWNVPMMGGDAA 252

Query: 251 VTNEYWAITGPAGENTMMTFGPD-PREMPEAKE----AVEKFRKAGYEPEGYTLYTYAAL 305
              +   I G A         P  P++   A+     A  K +        +++    A 
Sbjct: 253 NNLDLVKIAGKAAAKGYFFLSPPVPQDFDTAEAKAFLAAYKAKHNALPNSVWSVLAGDAF 312

Query: 306 QIWAEAAKQANSTDSAKIADVLRK--NSYNTVIGKIGFDAKGDVTSPAYVWYRWN 358
           ++  EA ++    D A IA  L+    +Y  + G+I F+ KGD     Y  Y  N
Sbjct: 313 KVIVEAVQKGGKADGAGIATYLKTQLKNYPGLSGQISFNEKGDRVGDLYRVYDVN 367


Lambda     K      H
   0.312    0.129    0.366 

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: 376
Number of extensions: 24
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: 366
Length of database: 376
Length adjustment: 30
Effective length of query: 336
Effective length of database: 346
Effective search space:   116256
Effective search space used:   116256
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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