GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Collimonas pratensis Ter91

Align Ribose import permease protein RbsC (characterized)
to candidate WP_061938906.1 CPter91_RS07340 ABC transporter permease

Query= SwissProt::P0AGI1
         (321 letters)



>NCBI__GCF_001584185.1:WP_061938906.1
          Length = 343

 Score =  236 bits (602), Expect = 6e-67
 Identities = 136/314 (43%), Positives = 204/314 (64%), Gaps = 16/314 (5%)

Query: 13  TKAWLMEQKSLIALLVLIAIVSTLSPNFFTINNLFNILQQTSVNAIMAVGMTLVILTSGI 72
           T+  L+   SL+AL+V  +  S+   NF  I+NL +ILQ T+VN ++A+  T VI+T+GI
Sbjct: 30  TRQKLLAFASLLALMVFFSFASS---NFLEIDNLVSILQSTAVNGVLAIACTFVIITAGI 86

Query: 73  DLSVGSLL---ALTGAVAASIVGIEVNALVAVAAALALGAAIGAVTGVIVAKGRVQAFIA 129
           DLSVG+L+   A+   V  + +G+ +   + + AA+  GA  G V+GV+VAK ++  FIA
Sbjct: 87  DLSVGTLMTFCAVMAGVFLTYMGLPI--YIGIVAAVFFGALCGWVSGVLVAKLKIPPFIA 144

Query: 130 TLVMMLLLRGVTMVYTNGSPV----NTGFT--ENADLFGWFGIGRPLGVPTPVWIMGIVF 183
           TL MM+LL+G+++V +   P+      GF+      L G   +   L +P  V I+ +V 
Sbjct: 145 TLGMMMLLKGLSLVISGTKPIYFNDTPGFSAISQDSLIG--SLIPVLPIPNAVLILFLVA 202

Query: 184 LAAWYMLHHTRLGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGIIEVARLS 243
           + A  +L+ T  GRY +ALG NE A RLSG+NV+  K+ +Y+  G +  +AG++  +RL+
Sbjct: 203 IGAGIILNKTIFGRYTFALGSNEEALRLSGVNVDFWKVAIYTFSGAICGIAGLLIASRLN 262

Query: 244 SAQPTAGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQM 303
           SAQP  G GYELDAIAAVV+GGTSL+GG G I+GT+IGA I+  L NGL ++ V+  +Q 
Sbjct: 263 SAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLINGLRMMSVAQEWQT 322

Query: 304 IVKAVVILLAVLVD 317
           +V  V+I+LAV +D
Sbjct: 323 VVTGVIIILAVYMD 336


Lambda     K      H
   0.324    0.139    0.393 

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: 245
Number of extensions: 8
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 321
Length of database: 343
Length adjustment: 28
Effective length of query: 293
Effective length of database: 315
Effective search space:    92295
Effective search space used:    92295
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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