GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Rhodomicrobium vannielii ATCC 17100

Align leucine-specific-binding protein LivK (characterized)
to candidate WP_013418499.1 RVAN_RS04095 branched-chain amino acid ABC transporter substrate-binding protein

Query= CharProtDB::CH_107418
         (369 letters)



>NCBI__GCF_000166055.1:WP_013418499.1
          Length = 366

 Score =  266 bits (680), Expect = 7e-76
 Identities = 145/357 (40%), Positives = 216/357 (60%), Gaps = 4/357 (1%)

Query: 6   KTIIAGM--IALAISHTAMADDIKVAVVGAMSGPIAQWGDMEFNGARQAIKDINAKGGIK 63
           + I+AG+  + L  +  A ADDI +A+ G M+G  A +G     G   A+ DINAKGG+ 
Sbjct: 2   RAILAGLTLLGLGAAAPAWADDISIAIAGPMTGKEATFGAQFKAGGEAAVADINAKGGVL 61

Query: 64  GDKLVGVEYDDACDPKQAVAVANKIVNDGIKYVIGHLCSSSTQPASDIYEDEGILMISPG 123
           G +L     DD CDPKQA AVA ++ + G+ +V GH CSSS+ PAS +Y ++GI+ ISPG
Sbjct: 62  GKQLKLEMGDDQCDPKQARAVAEQLSSSGVAFVAGHFCSSSSIPASSVYNEQGIVQISPG 121

Query: 124 ATNPELT-QRGYQHIMRTAGLDSSQGPTAAKYILETVKPQRIAIIHDKQQYGEGLARSVQ 182
           +TNP+LT +R      R  G D  QG  A  Y+ +    ++IAI+HDK  YG+GLA   +
Sbjct: 122 STNPKLTDERPGDFTYRMCGRDDQQGGVAGAYLAKEFADKKIAILHDKTAYGQGLADETK 181

Query: 183 DGLKAANANVVFFDGITAGEKDFSALIARLKKENIDFVYYGGYYPEMGQMLRQARSVGLK 242
             L AA    VF++ IT GEKD++A++ +LK+  +D VY GGY+ E G ++RQ R+ G+K
Sbjct: 182 KALNAAGKQEVFYEAITPGEKDYTAVVTKLKQNGVDVVYLGGYHTEGGLIIRQMRAQGMK 241

Query: 243 TQFMGPEGVGNASLSNIAGDAAEGMLVTMPKRYDQDPANQGIVDALKADKKDPSGPYVWI 302
           T  +G + + +  L +IAGD  EG ++T      ++PA + +V+AL+    +P G YV  
Sbjct: 242 TILVGGDALVSTELGSIAGDDVEGTMMTFSPDPRKNPAAKEVVEALEKKGINPEG-YVVY 300

Query: 303 TYAAVQSLATALERTGSDEPLALVKDLKANGANTVIGPLNWDEKGDLKGFDFGVFQW 359
           TYAA+Q+ A A E+ GS E   +V  +K    +T +G   +D KGD     +  ++W
Sbjct: 301 TYAAIQTWAQAAEKAGSIEGDKVVVAMKDLEFDTALGKFKFDAKGDPNLPSYVFYRW 357


Lambda     K      H
   0.315    0.133    0.386 

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: 388
Number of extensions: 18
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: 369
Length of database: 366
Length adjustment: 30
Effective length of query: 339
Effective length of database: 336
Effective search space:   113904
Effective search space used:   113904
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 (21.5 bits)
S2: 49 (23.5 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