GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_068173840.1 HTA01S_RS16515 ABC transporter ATP-binding protein

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_001592305.1:WP_068173840.1
          Length = 361

 Score =  530 bits (1365), Expect = e-155
 Identities = 264/361 (73%), Positives = 312/361 (86%), Gaps = 5/361 (1%)

Query: 1   MKNTKTN----WIIGAVALLVLPLILQSFG-NAWVRIADLALLYVLLALGLNIVVGYAGL 55
           M NTK+     +++   ALL+LP++LQS G N+WVRI D+ALLYVLLALGLNIVVGYAGL
Sbjct: 1   MMNTKSGKLIVFLLAGAALLLLPILLQSTGSNSWVRILDIALLYVLLALGLNIVVGYAGL 60

Query: 56  LDLGYVAFYAVGAYLFALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAM 115
           LDLGY+AF+AVGAY+FAL+ SPHL D F A  AMFP GLH S+WIV+ +AA++A   G +
Sbjct: 61  LDLGYIAFFAVGAYVFALLGSPHLIDTFPAIKAMFPEGLHISIWIVMIIAAVIAGVVGMI 120

Query: 116 LGAPTLKLRGDYLAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKR 175
           LGAPTLKLRGDYLAI+TLGFGEIIRIFL N+D PVN+TNGPKG+ QID++ VFGLDLG+R
Sbjct: 121 LGAPTLKLRGDYLAIITLGFGEIIRIFLLNMDRPVNITNGPKGISQIDTISVFGLDLGQR 180

Query: 176 LEVFGFDINSVTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRN 235
           L +  +    VTLYYYLFL  VV +VI+ YRLQDSRIGRAWMAIREDEIAAKAMG+NTRN
Sbjct: 181 LTIGDYSFQPVTLYYYLFLFFVVGAVILSYRLQDSRIGRAWMAIREDEIAAKAMGLNTRN 240

Query: 236 MKLLAFGMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAV 295
           +KLLAFGMGA+FGGVSG +F +FQ FVSPESFSLMESVM+VAMVVLGGIGHIPGVILGA+
Sbjct: 241 LKLLAFGMGATFGGVSGVLFASFQRFVSPESFSLMESVMVVAMVVLGGIGHIPGVILGAL 300

Query: 296 LLSALPEVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGLWPSPEHGKSLT 355
           LL+ LPE+LR+VA PL AMTDGRL   ILRQLLIALAM+++ML+RP+GLWP+PEHGKSL+
Sbjct: 301 LLAGLPELLRHVAHPLTAMTDGRLAPEILRQLLIALAMVVVMLIRPKGLWPAPEHGKSLS 360

Query: 356 Q 356
           +
Sbjct: 361 K 361


Lambda     K      H
   0.328    0.144    0.430 

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: 476
Number of extensions: 16
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: 358
Length of database: 361
Length adjustment: 29
Effective length of query: 329
Effective length of database: 332
Effective search space:   109228
Effective search space used:   109228
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: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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