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_012631044.1 MNOD_RS38640 substrate-binding domain-containing protein

Query= uniprot:A0A0N9WNI6
         (308 letters)



>NCBI__GCF_000022085.1:WP_012631044.1
          Length = 307

 Score =  254 bits (650), Expect = 1e-72
 Identities = 145/303 (47%), Positives = 196/303 (64%), Gaps = 6/303 (1%)

Query: 10  LALSLMLASGAALADLRIGVSMSQFDDTWLTYLRESMDKQAKSMPDGVKLQFEDARSDVV 69
           LA +L   +  A A  RIGVSM+  D+ +LT L   M  +A +   GV+L  EDA+ DV 
Sbjct: 6   LAAALTACALPAYAGGRIGVSMTSLDNPFLTILLNGMKGEA-ARTKGVELMLEDAQRDVS 64

Query: 70  KQLSQVESFISQKVDAIVVNPVDTAATRKITEAAVKAGIPLVYVNRRPDDLK--LPKGVI 127
           +QLSQV++F++ +VDAIVVN VD  +T  IT AA  AGIPLVYVN  P +L   +PKG  
Sbjct: 65  RQLSQVQNFVANRVDAIVVNAVDGDSTAAITRAAKAAGIPLVYVNHPPAELGRGMPKGTA 124

Query: 128 TVASNDLEAGQMQMQYLAEKMKGKGDIVILLGDLANNSTTNRTKGVKEVLAKYPG--IKI 185
            V SN+L++G MQ + + + + GKG  VIL+G L N+S   RTK V +V  + P   I I
Sbjct: 125 FVGSNELDSGTMQARAVCKMLAGKGRAVILMGPLENHSALVRTKDVVDVF-RTPDCPIHI 183

Query: 186 DQEQTGTWSRDKGMTLVNDWLTQGRKFDAIVSNNDEMAIGAAMALKQAGVEKGSVLIAGV 245
             +QT  W R +   LV  WLT G +FDA+++N+DEMAIGAA ALK AGV    V+IAG+
Sbjct: 184 LDKQTANWMRVEAQDLVASWLTAGMRFDAVIANSDEMAIGAAQALKSAGVAMKDVVIAGI 243

Query: 246 DGTPDGLRAVKKGDLAVSVFQDANGQAVDSIDAAVKMAKNEPVEQAVWVPYRLITPENVD 305
           D TPDGL A+  GDL V+VFQ+A  Q   ++  AV MA  E  E A+WVP+ L+T +N+ 
Sbjct: 244 DATPDGLAAMATGDLDVTVFQNATRQGEVAVQTAVAMAAGEKAEDAIWVPFELVTKDNLA 303

Query: 306 QFK 308
           +++
Sbjct: 304 EYR 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: 249
Number of extensions: 10
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: 307
Length adjustment: 27
Effective length of query: 281
Effective length of database: 280
Effective search space:    78680
Effective search space used:    78680
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