Alignments for a candidate for actP in Desulfovibrio vulgaris Hildenborough

GapMind for catabolism of small carbon sources

Alignments for a candidate for actP in Desulfovibrio vulgaris Hildenborough

Align Acetate permease; SubName: Full=Actetate permease; SubName: Full=Cation acetate symporter; SubName: Full=Cation/acetate symporter (characterized, see rationale)
to candidate 209382 DVU0446 sodium/solute symporter family protein

Query= uniprot:A0A1N7U9G2
         (552 letters)



>MicrobesOnline__882:209382
          Length = 515

 Score =  576 bits (1484), Expect = e-169
 Identities = 305/513 (59%), Positives = 381/513 (74%), Gaps = 10/513 (1%)

Query: 34  NVSAIVMFVVFVGATLCITYWASKRNKSAADYYAAGGKITGFQNGLAIAGDYMSAASFLG 93
           N  +I+ F  FV  TL IT++A++R++SA+++YAAG  +TG QNGLA+AGDYMSAASFLG
Sbjct: 12  NAVSILFFFAFVAFTLAITWFAARRSRSASEFYAAGRSVTGLQNGLALAGDYMSAASFLG 71

Query: 94  ISALVYTSGYDGLIYSIGFLVGWPIILFLIAERLRNLGKYTFADVASYRLGQTQIRSLSA 153
           I+ LV   GYDGLIYSIGFLVGWP+++FLIAE LRNLG+YTFADV +YRL Q  IR  +A
Sbjct: 72  IAGLVSLKGYDGLIYSIGFLVGWPLMMFLIAEPLRNLGRYTFADVVAYRLRQKPIRIAAA 131

Query: 154 CGSLVVVAFYLIAQMVGAGKLIQLLFGLDYHVAVILVGILMVLYVLFGGMLATTWVQIIK 213
           CGSL+ V FYLIAQMVG+G L+QL+FG+ Y  AV+ VG +M+ YVLFGGMLATTWVQI K
Sbjct: 132 CGSLMTVCFYLIAQMVGSGALVQLMFGIRYEYAVVAVGFIMMAYVLFGGMLATTWVQITK 191

Query: 214 AVLLLSGASFMALMVMKHVNFDFNALFSEAIKVHPKGEAIMSPGGLVKDPISAFSLGLAL 273
           AVLLL GA+ M +MV+   ++    LF  A   H  GEA+++PGGLV +P  A SLG+AL
Sbjct: 192 AVLLLGGATAMVVMVLAQFDYSPTRLFVTAAAKH--GEAMLAPGGLVSNPWDAISLGMAL 249

Query: 274 MFGTAGLPHILMRFFTVSDAKEARKSVFYATGFIGYFYILTFIIGFGAILLVSTNPAFKD 333
           MFGTAGLPHILMRF+TV DA+ ARKSVFYATG I YFY+LTFIIGFGA++LV       D
Sbjct: 250 MFGTAGLPHILMRFYTVPDARAARKSVFYATGLISYFYVLTFIIGFGAMMLVG-----PD 304

Query: 334 AAGALMGGNNMAAVHLANAVGGSIFLGFISAVAFATILAVVAGLTLAGASAVSHDLYASV 393
           A      G NMAA  LA   GG++FLGFI+AVAFATILAVVAGLTLAGA+  SHDLYA+V
Sbjct: 305 AIRMFDKGGNMAAPLLAEVTGGTMFLGFIAAVAFATILAVVAGLTLAGATTFSHDLYANV 364

Query: 394 IKKGKANDKDEIRVSKITTIALGVLAIGLGILFESQNIAFMVGLAFSIAASCNFPVLLLS 453
            K G++N+ DE+RV+K  TIALGV+A+ LGI F+ QN+AFMVGLAF+IAAS N P LLLS
Sbjct: 365 FKGGQSNEADEVRVAKRATIALGVIAMLLGIAFKGQNVAFMVGLAFAIAASANLPALLLS 424

Query: 454 MYWKNLTTRGAMIGGWLGLVSAVGLMVLGPTIWVSILHHEKAIFPYEYPALFSMIIAFVG 513
           + W+  +T GA+     G V AVGL+++ PT+W  + H   A FP + PAL SM  AF+ 
Sbjct: 425 IMWRGCSTTGAVWAIVTGGVLAVGLIIVSPTVWTDVFHLGTAPFPLKNPALLSMPAAFMA 484

Query: 514 IWFFSITDKSSAAEKERALYFPQFVRSQTGLGS 546
               S+    S   +E A +  Q +R+  G+G+
Sbjct: 485 GIAGSLLRPDS---EESARFDAQKIRNYLGVGA 514


Lambda     K      H
   0.327    0.140    0.415 

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: 866
Number of extensions: 41
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: 552
Length of database: 515
Length adjustment: 35
Effective length of query: 517
Effective length of database: 480
Effective search space:   248160
Effective search space used:   248160
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 52 (24.6 bits)

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

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources