GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Thauera aminoaromatica S2

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_004321583.1 C665_RS15465 high-affinity branched-chain amino acid ABC transporter permease LivM

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_000310185.1:WP_004321583.1
          Length = 443

 Score =  256 bits (653), Expect = 1e-72
 Identities = 159/350 (45%), Positives = 205/350 (58%), Gaps = 48/350 (13%)

Query: 9   IIGAVAL---LVLPLILQSFGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYA 65
           ++G VAL   + LP++  S     V  A   L+YV+L  GLN+VVG AGLLDLGYVAFYA
Sbjct: 104 VLGWVALGASIALPIVF-SDNRYVVDTATTVLIYVMLGWGLNVVVGLAGLLDLGYVAFYA 162

Query: 66  VGAYLFALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRG 125
           VGAY +AL+++                    S W  +PV+  LAA FG +LG P L+LRG
Sbjct: 163 VGAYSYALLSTQ----------------FGWSFWEALPVSGALAASFGILLGYPILRLRG 206

Query: 126 DYLAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLE-------- 177
           DYLAIVTLGFGEIIRI L N       +NGP G+  I     FGLD  +           
Sbjct: 207 DYLAIVTLGFGEIIRIILVNW---TEFSNGPNGISSIPRPSFFGLDFTRSAPEGGQTFAG 263

Query: 178 VFGFD---INSVTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTR 234
            FG +   ++ +   YYL LVL +++     RL+   +GRAW A+REDEIA +AMG+NT 
Sbjct: 264 FFGLEFSPMHRLIFLYYLILVLALLTHAFVSRLRKLPVGRAWEALREDEIACQAMGMNTT 323

Query: 235 NMKLLAFGMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGA 294
           N+KL AF +GA  GG +G  F A QGF+SPESF+  ES +I+A+VVLGG+G   GV+L A
Sbjct: 324 NIKLSAFAIGAMLGGFAGVFFAARQGFISPESFTFTESAIILAIVVLGGMGSQMGVVLAA 383

Query: 295 VLLSALPEVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGL 344
            LL  +PE  R              + A  R LL  LAM++IM+ RP GL
Sbjct: 384 TLLVLIPEFGR--------------NFAEYRMLLFGLAMVLIMVWRPGGL 419


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: 444
Number of extensions: 25
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: 358
Length of database: 443
Length adjustment: 31
Effective length of query: 327
Effective length of database: 412
Effective search space:   134724
Effective search space used:   134724
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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