GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Rhodomicrobium vannielii ATCC 17100

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate WP_013418499.1 RVAN_RS04095 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>NCBI__GCF_000166055.1:WP_013418499.1
          Length = 366

 Score =  426 bits (1096), Expect = e-124
 Identities = 207/344 (60%), Positives = 260/344 (75%), Gaps = 1/344 (0%)

Query: 24  DIAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGVLGQKLKLEVGDDACDPKQAVAV 83
           DI++A AGP+TG+ ATFG Q K G E AVADINA GGVLG++LKLE+GDD CDPKQA AV
Sbjct: 23  DISIAIAGPMTGKEATFGAQFKAGGEAAVADINAKGGVLGKQLKLEMGDDQCDPKQARAV 82

Query: 84  ANQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISPASTNPKLTEQNLKN-VFRVCGR 142
           A QL+ +GV FVAGHFCS SSIPAS VY E+G++QISP STNPKLT++   +  +R+CGR
Sbjct: 83  AEQLSSSGVAFVAGHFCSSSSIPASSVYNEQGIVQISPGSTNPKLTDERPGDFTYRMCGR 142

Query: 143 DDQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQKALNAGGQKEKIYEAYTAGEK 202
           DDQQG +AG YL + +  K +AILHDK+AYG+GLADET+KALNA G++E  YEA T GEK
Sbjct: 143 DDQQGGVAGAYLAKEFADKKIAILHDKTAYGQGLADETKKALNAAGKQEVFYEAITPGEK 202

Query: 203 DYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLNAPIVSGDALVTNEYWAITGPA 262
           DY+A+V+KLKQ  VDVVY+GGYHTE GL+ RQM+ QG+   +V GDALV+ E  +I G  
Sbjct: 203 DYTAVVTKLKQNGVDVVYLGGYHTEGGLIIRQMRAQGMKTILVGGDALVSTELGSIAGDD 262

Query: 263 GENTMMTFGPDPREMPEAKEAVEKFRKAGYEPEGYTLYTYAALQIWAEAAKQANSTDSAK 322
            E TMMTF PDPR+ P AKE VE   K G  PEGY +YTYAA+Q WA+AA++A S +  K
Sbjct: 263 VEGTMMTFSPDPRKNPAAKEVVEALEKKGINPEGYVVYTYAAIQTWAQAAEKAGSIEGDK 322

Query: 323 IADVLRKNSYNTVIGKIGFDAKGDVTSPAYVWYRWNNGQYAQVK 366
           +   ++   ++T +GK  FDAKGD   P+YV+YRW    Y Q++
Sbjct: 323 VVVAMKDLEFDTALGKFKFDAKGDPNLPSYVFYRWGKKNYEQIQ 366


Lambda     K      H
   0.312    0.129    0.366 

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: 472
Number of extensions: 21
Number of successful extensions: 2
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: 366
Length of database: 366
Length adjustment: 30
Effective length of query: 336
Effective length of database: 336
Effective search space:   112896
Effective search space used:   112896
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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