GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Methylobacterium nodulans ORS 2060

Align Fructose import permease protein FruG (characterized)
to candidate WP_012631047.1 MNOD_RS38655 ABC transporter permease

Query= SwissProt::Q8G845
         (340 letters)



>NCBI__GCF_000022085.1:WP_012631047.1
          Length = 344

 Score =  133 bits (334), Expect = 7e-36
 Identities = 100/316 (31%), Positives = 162/316 (51%), Gaps = 36/316 (11%)

Query: 26  LAAVVIFILMIIMGQALFGTYIRLGFISSLFIDHAYLIILAVAMTLPILTGGIDLSVGAI 85
           +A V   +  +++GQ+      RL   + L +  + + I+A+ +T  I+TGGIDLS G++
Sbjct: 36  IALVFELLGWVVVGQSFLMNPQRL---TILILQVSVIGIIAIGVTQVIITGGIDLSSGSV 92

Query: 86  VAITAVVGLKLANAG------------VPAFLVMIIMLLIGAVFGLLAGTLIEEFNMQPF 133
           V ++A+V    A +             +P  + +++ L IG + G++ G LI    + PF
Sbjct: 93  VGLSAMVAASDAQSSAWTKVLYPSMTDLPVAVPILVGLAIGLLAGVINGMLIVYTKIPPF 152

Query: 134 IATLSTMFLARGLASIISTDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFNVGVIIALV 193
           IATL  M  ARGL+   +         ++FS I + I                 V+I L 
Sbjct: 153 IATLGMMVSARGLSKWYTKGQPVSGLTDEFSVIGSGIW---------------PVVIFLS 197

Query: 194 VVVFGYVFLHHTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAALASIVYTAN 253
           V V  +V L +TR G+  YAIG +  +A + G+ V R    +Y  +  L  LA IV  A 
Sbjct: 198 VAVIFHVLLRYTRYGKFTYAIGANEQAARISGIEVDRHLIKVYGVAGLLGGLAGIVTAAR 257

Query: 254 IGSAKNTVGVGWELDAVASVVIGGTIITGGFGYVLGSVLGSLVRSILDPLTSDF---GVP 310
             +A+  +G  +ELDA+A+ VIGG  ++GG G + G+V+G++   IL  +TS F    V 
Sbjct: 258 AQTAQAGMGTMYELDAIAAAVIGGASLSGGVGRITGTVIGTI---ILGTMTSGFTFLRVD 314

Query: 311 AEWTTIVIGLMILVFV 326
           A +  I+ GL+I+  V
Sbjct: 315 AFYQEIIKGLIIIAAV 330


Lambda     K      H
   0.327    0.142    0.400 

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: 280
Number of extensions: 21
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: 340
Length of database: 344
Length adjustment: 29
Effective length of query: 311
Effective length of database: 315
Effective search space:    97965
Effective search space used:    97965
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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