GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11885 in Sinorhizobium fredii NGR234

Align Rhizopine-binding protein (characterized, see rationale)
to candidate WP_015888123.1 NGR_RS09870 sugar ABC transporter substrate-binding protein

Query= uniprot:A0A0N9WNI6
         (308 letters)



>NCBI__GCF_000018545.1:WP_015888123.1
          Length = 309

 Score =  277 bits (709), Expect = 2e-79
 Identities = 147/301 (48%), Positives = 213/301 (70%), Gaps = 6/301 (1%)

Query: 11  ALSLMLASGAALADLRIGVSMSQFDDTWLTYLRESMDKQAKSMPDGVKLQFEDARSDVVK 70
           A+++M+++ A      IGVSM+ FDD +LT LR  M   AK++ +GV+LQ EDA++DV K
Sbjct: 9   AMAVMMSTAAHAET--IGVSMALFDDNFLTVLRNGMQDYAKTL-NGVELQIEDAQNDVAK 65

Query: 71  QLSQVESFISQKVDAIVVNPVDTAATRKITEAAVKAGIPLVYVNRRPDDL-KLPKGVITV 129
           Q SQ+++FI+  VDAI+VNPVDT AT  +++ A  AGIPLVYVNR P ++  LP+    V
Sbjct: 66  QQSQIQNFIAAGVDAIIVNPVDTDATAAMSKIAADAGIPLVYVNREPVNIDSLPEKQAFV 125

Query: 130 ASNDLEAGQMQMQYLAEKMKGKGDIVILLGDLANNSTTNRTKGVKEVLAK--YPGIKIDQ 187
           ASN++E+G ++ Q + + + GKG  V+++G+L+N +   RTK + +VLA     GI+I +
Sbjct: 126 ASNEMESGTLETQEVCKLLGGKGKAVVMMGELSNQAARMRTKDIHDVLATDACKGIEIIE 185

Query: 188 EQTGTWSRDKGMTLVNDWLTQGRKFDAIVSNNDEMAIGAAMALKQAGVEKGSVLIAGVDG 247
           EQT  WSR +G  LV +WL+ G +FDA+++NNDEMAIGA  ALK AG    SV+I GVD 
Sbjct: 186 EQTANWSRTQGADLVTNWLSAGLEFDAVIANNDEMAIGAIQALKAAGRSMDSVVIGGVDA 245

Query: 248 TPDGLRAVKKGDLAVSVFQDANGQAVDSIDAAVKMAKNEPVEQAVWVPYRLITPENVDQF 307
           T D L A+  GDL V+VFQ+A GQ   S+D A+K+AK E VE+ V++P+ L+T EN+D++
Sbjct: 246 TQDALAAMAAGDLDVTVFQNAAGQGQGSVDTALKLAKGETVEKKVYIPFELVTKENLDKY 305

Query: 308 K 308
           +
Sbjct: 306 Q 306


Lambda     K      H
   0.315    0.130    0.360 

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: 263
Number of extensions: 15
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: 308
Length of database: 309
Length adjustment: 27
Effective length of query: 281
Effective length of database: 282
Effective search space:    79242
Effective search space used:    79242
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.5 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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