GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11885 in Methylobacterium nodulans ORS 2060

Align Rhizopine-binding protein (characterized, see rationale)
to candidate WP_012631049.1 MNOD_RS38665 sugar ABC transporter substrate-binding protein

Query= uniprot:A0A0N9WNI6
         (308 letters)



>NCBI__GCF_000022085.1:WP_012631049.1
          Length = 313

 Score =  254 bits (648), Expect = 2e-72
 Identities = 142/306 (46%), Positives = 208/306 (67%), Gaps = 9/306 (2%)

Query: 10  LALSLMLASGAALADLRIGVSMSQFDDTWLTYLRESMDKQAKSMPDGVKLQFEDARSDVV 69
           +A+ +   + +ALA+  IGVSMS FDD  LT +R  M   A ++ +GV LQ EDA++DV 
Sbjct: 7   VAVLMSSIASSALAE-NIGVSMSLFDDNLLTVMRNDMTNYATTL-NGVTLQIEDAQNDVA 64

Query: 70  KQLSQVESFISQKVDAIVVNPVDTAATRKITEAAVKAGIPLVYVNRRPDDL-KLPKGVIT 128
           KQ SQV++FI+  VDAI+VNPVDT AT  I++ A  AGIPLVYVNR P +L KLP     
Sbjct: 65  KQQSQVQNFIAAGVDAIIVNPVDTDATAAISKIASNAGIPLVYVNRLPVNLGKLPPKQAF 124

Query: 129 VASNDLEAGQMQMQYLAEKMKGKG----DIVILLGDLANNSTTNRTKGVKEVLA--KYPG 182
           V  ++ E+G +Q + +   +K  G    +IV+++G+L+N +   RT+ V EV+A  +   
Sbjct: 125 VGPDERESGTLQTKEICRLLKQAGKTKANIVVMMGELSNQAARQRTQDVHEVIATPECSF 184

Query: 183 IKIDQEQTGTWSRDKGMTLVNDWLTQGRKFDAIVSNNDEMAIGAAMALKQAGVEKGSVLI 242
           +KI +EQT  WSR +G  L+++WL+ G +FDA+VSNNDEMAIGA  A+K A V+  ++++
Sbjct: 185 MKIVEEQTANWSRTQGADLMSNWLSAGVQFDAVVSNNDEMAIGAIQAMKAARVDMKTMIV 244

Query: 243 AGVDGTPDGLRAVKKGDLAVSVFQDANGQAVDSIDAAVKMAKNEPVEQAVWVPYRLITPE 302
            GVD T D L A+  GDL V+VFQ+  GQ   ++DAA+K+A+ + VEQ V+VP+ L+TP 
Sbjct: 245 GGVDATQDALAAMAAGDLDVTVFQNVVGQGRGALDAALKLARGKKVEQKVFVPFELVTPA 304

Query: 303 NVDQFK 308
           N+  ++
Sbjct: 305 NLQNYR 310


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: 253
Number of extensions: 13
Number of successful extensions: 4
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: 308
Length of database: 313
Length adjustment: 27
Effective length of query: 281
Effective length of database: 286
Effective search space:    80366
Effective search space used:    80366
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.

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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