GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Mesorhizobium ciceri biovar biserrulae WSM1271

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate WP_013528427.1 MESCI_RS02785 branched-chain amino acid ABC transporter permease

Query= uniprot:Q1MCU0
         (300 letters)



>NCBI__GCF_000185905.1:WP_013528427.1
          Length = 300

 Score =  191 bits (485), Expect = 2e-53
 Identities = 101/299 (33%), Positives = 177/299 (59%), Gaps = 17/299 (5%)

Query: 1   MEYFVQQLLNGLTLGSIYGLVAIGYTMVYGIIGMINFAHGDIFMLGGFAALIVFLVLTSI 60
           ++Y +QQ++N ++LGS+Y LVA+G ++V+G++ + NFAHGD+ M+G F   +    L  I
Sbjct: 4   LDYILQQIVNAVSLGSLYALVAVGLSIVFGVLKLTNFAHGDVMMVGAFGVAL----LVGI 59

Query: 61  FAGLPVAVLLLVMLVVAMLMTSLWNWTIERVAYRPLRGSFRLAPLITAIGMSITLSN--F 118
               PVAV      +  +   ++  + IER+AYRP+R +  +A L+T++ ++  + N   
Sbjct: 60  GVPFPVAV------ICGIAAAAVAGFLIERIAYRPIRDAPDVARLLTSLAVTYIIENVGI 113

Query: 119 IQVTQGPRNKPIPPMVSSVYQFGNISVSLKQI--IIIVITAVLLTIFWYIVNRTALGRAQ 176
           +  T  PRN P+P ++++ ++  N +++   I  + I +T V L +  + + RT  G   
Sbjct: 114 LVFTSSPRNFPLPDILNTSWEMSNGAITFTSINLLTIALTFVSLLLLGWFITRTTTGLGM 173

Query: 177 RATEQDRKMAALLGVNVDQTISITFVMGAALAAVAGTMYLMYYGVASFNDGFTPGVKAFT 236
           RA  +D   A L+G+NV++ I + F++ +A A +AG ++    GV     GFTP +KAF 
Sbjct: 174 RAAAEDMSAAHLVGLNVNRLIIVAFIVASAYAGLAGILWAAQAGVVQPQMGFTPLLKAFV 233

Query: 237 AAVLGGIGSLPGAVFGGLLIGLIESLWSAYF---TIAYKDVATFAILAFVLIFKPTGIL 292
           AA++GG GS+ GA+ GG ++G +E    A+      +Y+D   FA+L   L+ +P G+L
Sbjct: 234 AAIIGGFGSIAGALVGGYILGALEIFIVAFLPSSVSSYRDAIVFAVLIAFLLVRPGGLL 292


Lambda     K      H
   0.329    0.143    0.421 

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: 298
Number of extensions: 21
Number of successful extensions: 5
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: 300
Length of database: 300
Length adjustment: 27
Effective length of query: 273
Effective length of database: 273
Effective search space:    74529
Effective search space used:    74529
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: 48 (23.1 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