GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Collimonas pratensis Ter91

Align Monosaccharide-transporting ATPase; EC 3.6.3.17 (characterized, see rationale)
to candidate WP_061938906.1 CPter91_RS07340 ABC transporter permease

Query= uniprot:B2SYR4
         (338 letters)



>NCBI__GCF_001584185.1:WP_061938906.1
          Length = 343

 Score =  188 bits (477), Expect = 2e-52
 Identities = 111/321 (34%), Positives = 183/321 (57%), Gaps = 13/321 (4%)

Query: 26  KAKWWQQITEYSLIVI--FVVMFATMSLTVDHFFSIENMLGLALSISQIGMVSCTMMFCL 83
           KAK +   T   L+     + +    S    +F  I+N++ +  S +  G+++    F +
Sbjct: 22  KAKIFHPATRQKLLAFASLLALMVFFSFASSNFLEIDNLVSILQSTAVNGVLAIACTFVI 81

Query: 84  ASRDFDLSVGSTVAFAGVLCAMVLNATG-NTFIAIVAAVAAGGVIGFVNGAVIAYLRINA 142
            +   DLSVG+ + F  V+  + L   G   +I IVAAV  G + G+V+G ++A L+I  
Sbjct: 82  ITAGIDLSVGTLMTFCAVMAGVFLTYMGLPIYIGIVAAVFFGALCGWVSGVLVAKLKIPP 141

Query: 143 LITTLATMEIVRGLGFIVSHGQAVGVSSDT--FIALGGLSFFGVSLPIW----VTLLCFI 196
            I TL  M +++GL  ++S  + +   +DT  F A+   S  G  +P+       L+ F+
Sbjct: 142 FIATLGMMMLLKGLSLVISGTKPI-YFNDTPGFSAISQDSLIGSLIPVLPIPNAVLILFL 200

Query: 197 VF---GVMLNQTVYGRNTLAIGGNPEASRLAGINVERTRVYIFLIQGAVTALAGVILASR 253
           V    G++LN+T++GR T A+G N EA RL+G+NV+  +V I+   GA+  +AG+++ASR
Sbjct: 201 VAIGAGIILNKTIFGRYTFALGSNEEALRLSGVNVDFWKVAIYTFSGAICGIAGLLIASR 260

Query: 254 ITSGQPNAAQGFELNVISACVLGGVSLLGGRATISGVVIGVLIMGTVENVMNLMNIDAFY 313
           + S QP   QG+EL+ I+A V+GG SL GG  TI G +IG  IM  + N + +M++   +
Sbjct: 261 LNSAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLINGLRMMSVAQEW 320

Query: 314 QYLVRGAILLAAVLLDQLKNR 334
           Q +V G I++ AV +D L+ R
Sbjct: 321 QTVVTGVIIILAVYMDILRRR 341


Lambda     K      H
   0.326    0.139    0.396 

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: 312
Number of extensions: 18
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: 338
Length of database: 343
Length adjustment: 28
Effective length of query: 310
Effective length of database: 315
Effective search space:    97650
Effective search space used:    97650
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: 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