GapMind for catabolism of small carbon sources

 

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

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_068167375.1 HTA01S_RS04365 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_001592305.1:WP_068167375.1
          Length = 358

 Score =  169 bits (429), Expect = 9e-47
 Identities = 111/324 (34%), Positives = 171/324 (52%), Gaps = 38/324 (11%)

Query: 93  LVALLVLAVAWPFMVSRGTVDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYAIGAYT 152
           L+ L +LA  W  ++    +   T  +IY ++GLGL ++ G +GL  LG+  F  +GAYT
Sbjct: 27  LLGLFLLAAPW--VIEEYWLAQLTFVLIYAVVGLGLMLLAGFTGLFSLGHAAFLGVGAYT 84

Query: 153 FALLNHYYGLGFWTCLPIAGLMAAAAGFLLGFPVLRLRGDYLAIVTLGFGEIVRILLLNN 212
            A++ +  GL F   L  AGL++AA G ++G P LR++G YL + TL FG IV   L   
Sbjct: 85  QAVMVNA-GLPFPLALACAGLLSAAVGMVVGLPALRVKGIYLGMATLAFGFIVEEALARW 143

Query: 213 TEITGGPNGISQIPKPTLFGLEFSRTAREGGWDTFSNFFGLKYDPSDRVIFLYLVALLLV 272
             +TGG +G+S  P P LFG E   T                          Y + L++ 
Sbjct: 144 ESVTGGNSGLSVNP-PALFGWELESTNE-----------------------FYFLCLVVT 179

Query: 273 VLSLFVINRLLRMPLGRAWEALREDEIACRSLGLSPRRIKLTAFTISAAFAGFAGTLFAA 332
           V +   I  L+R   GRA+ A+R+ EI+ +S+G+   R K  +F +SAA AG  G L+A 
Sbjct: 180 VGATLAIVNLMRSSTGRAFVAIRDSEISAQSMGIHLARYKTLSFALSAALAGIGGALYAH 239

Query: 333 RQGFVSPESFTFAESAFVLAIVVLGGMGSQFAVILAAILLVVSRELMRDFNEYSMLMLG- 391
           +  F+SPE F+  +S  +L +VV+GG+GS     L AI L+V  +L+    +Y    +G 
Sbjct: 240 KIQFLSPEQFSIIQSIDLLLMVVIGGLGSIHGAFLGAIFLIVMPQLIALGKDYLPDAIGQ 299

Query: 392 ---------GLMVL-MMIWRPQGL 405
                    GL+++  +++ P GL
Sbjct: 300 AAGLQGTVYGLVLIGFVLFEPMGL 323


Lambda     K      H
   0.330    0.145    0.436 

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: 316
Number of extensions: 16
Number of successful extensions: 4
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: 425
Length of database: 358
Length adjustment: 31
Effective length of query: 394
Effective length of database: 327
Effective search space:   128838
Effective search space used:   128838
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 (21.8 bits)
S2: 50 (23.9 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