GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Desulfovibrio vulgaris Hildenborough

Align TRAP dicarboxylate transport system, periplasmic component (DctP-like) (characterized, see rationale)
to candidate 208331 DVU2822 TRAP dicarboxylate family transporter

Query= uniprot:G8AR24
         (337 letters)



>MicrobesOnline__882:208331
          Length = 336

 Score =  170 bits (431), Expect = 4e-47
 Identities = 100/332 (30%), Positives = 182/332 (54%), Gaps = 6/332 (1%)

Query: 4   LRSVLLATGLAA-AILAPVAAS--AQDIKPRLIRFGYGLSESSNQGRAVKFFVEDMAKRS 60
           +R+   A  +AA A +A +AA   A+  K   IR  + ++  +N     + F E +  +S
Sbjct: 1   MRNFFKANAIAAIACIAMLAAGSYAEAAKRITIRLAHPMAPGNNVTLGYEKFKEIVEAKS 60

Query: 61  GGKLKVKGFADASLGSDIQMQNALIGGAQEMMVGSTATLVGIVKDFAVFDLPFLFNNEQE 120
            GK++++ F +  LGSD     A   G  EM   S+  +    K+  VFDLP++ + E +
Sbjct: 61  NGKVRIQLFGNCMLGSDRVTMEATQRGTLEMASSSSPNMTNFSKEMMVFDLPYITSPEHQ 120

Query: 121 AD---AVFDGPFGQKLAAKLNDKGLVGLVYWENGFRNLTNSKRPVEKVEDLKGIKLRVMQ 177
                A+ +G  G++L A     GL  ++Y E G+RN   +K+P++  +DLK +K+R   
Sbjct: 121 EKLYKALDEGALGERLDAIAAGIGLKPIMYSEYGYRNFATTKKPIKTADDLKNLKVRTTD 180

Query: 178 NPVYIDMFNGFGANAVPLSFSELFTAMETGTVDGQENPVTTIQSSKFYEVQKYLTISKHV 237
           +P+ + + +  G N  P+S+ E +TA++ GTVDG+ N    +  +K  EV ++   S H 
Sbjct: 181 SPIEVAVASALGMNPTPVSWGETYTALQQGTVDGEGNTFGLLNDAKHTEVLRHAMDSAHN 240

Query: 238 YSPWIVLASKRWYDGLSADERKIINEAAVASRDFERKDSREASKQSIAYLKDKGMQINEL 297
           YS  +++ +K ++D L AD ++I+ ++   +  ++R  S +  K++     ++G+ I +L
Sbjct: 241 YSMHLLMINKAYFDKLPADVQQILVDSGKEALAYQRAISNDLEKKAEQAFVERGIVITKL 300

Query: 298 SDAELGRMREMVKPAMDKFAADGGADLLNELQ 329
           +  E  +MRE+ +P  DKF+ D  ADL+  +Q
Sbjct: 301 APEERAKMRELTRPVWDKFSNDIPADLVKLVQ 332


Lambda     K      H
   0.317    0.134    0.372 

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: 235
Number of extensions: 9
Number of successful extensions: 2
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: 337
Length of database: 336
Length adjustment: 28
Effective length of query: 309
Effective length of database: 308
Effective search space:    95172
Effective search space used:    95172
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: 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