GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Roseburia faecis M72

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_022046731.1 M72_RS03885 ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_001406815.1:WP_022046731.1
          Length = 352

 Score =  191 bits (485), Expect = 2e-53
 Identities = 118/342 (34%), Positives = 194/342 (56%), Gaps = 24/342 (7%)

Query: 16  GKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTGELYFDDRLVASNGKL 75
           G   A D+V+  IE G+   +LGPSG+GKTT +R+IAGL+ P++G++Y D + V      
Sbjct: 13  GNFRASDHVSFGIEKGKLVALLGPSGSGKTTLLRMIAGLETPNSGDIYIDGQRVND---- 68

Query: 76  IVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKRVEEVAKILDIHHVLN 135
            VP   R IG VFQ +AL+  +T ++N+AF L   K+ K+EI+KRV E+ ++  +  +  
Sbjct: 69  -VPAAKRGIGFVFQNYALFRYMTVYDNVAFGLELAKVPKKEIKKRVTELLELTGLSGMEK 127

Query: 136 HFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSARALVKEVQSRLGVTLL 195
            +P +LSGGQ+QRVA ARAL  +P +LLLDEPF+ +DA++R   R  ++E+  +LG+T +
Sbjct: 128 RYPNQLSGGQRQRVAFARALAPNPQVLLLDEPFAAIDAKVRTELRNWLREMVVKLGITSI 187

Query: 196 VVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASLIGEINELEGKVTNEG 255
            V+HD  +   +AD + +   G + Q+G P ++Y +P +  VA  IG  + +E       
Sbjct: 188 FVTHDQDEAVEVADEIIITNHGHIEQMGTPMEIYKSPDTPFVAQFIGRSSIVEHYER--- 244

Query: 256 VVIGSLRFPVSVSSDRAIIGIRPEDVKLSKDVIKDDSWILVGKGKVKVIGYQGGLFRITI 315
                L F     +  A+  IRPE V++S+            +G VK + ++G    + +
Sbjct: 245 ----LLGFDPVEGATHAV--IRPEFVRMSRSE-PPQHMSAAERGIVKDVIFRGNHLDVVV 297

Query: 316 ----TPLDSEEEIFTYSDHPIHSGEEVLVYVRKDKIKVFEKN 353
                P+ +E  +      P+  GE+  VYV   ++ +F++N
Sbjct: 298 DVGGIPIVTERSL---EKDPVEIGEQ--VYVLIYRLYIFDEN 334


Lambda     K      H
   0.319    0.139    0.390 

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: 303
Number of extensions: 11
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: 353
Length of database: 352
Length adjustment: 29
Effective length of query: 324
Effective length of database: 323
Effective search space:   104652
Effective search space used:   104652
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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