GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Azospirillum brasilense Sp245

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate AZOBR_RS31205 AZOBR_RS31205 sugar ABC transporter permease

Query= SwissProt::P39328
         (341 letters)



>FitnessBrowser__azobra:AZOBR_RS31205
          Length = 354

 Score =  386 bits (992), Expect = e-112
 Identities = 201/304 (66%), Positives = 245/304 (80%)

Query: 22  MPQLVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPIDILNRAAPVALLAIGMTLVIATGG 81
           +PQ  AL  VLL + L+ P F+ + LQDGRLFGS ID+LNR APVALLAIGMT+VIAT G
Sbjct: 12  LPQYGALAAVLLANWLLFPDFFSIRLQDGRLFGSLIDVLNRGAPVALLAIGMTMVIATRG 71

Query: 82  IDLSVGAVMAIAGATTAAMTVAGFSLPIVLLSALGTGILAGLWNGILVAILKIQPFVATL 141
           +DLSVGAVMAI+GA  A +T AG+ L  VL ++L  G+L GLWNG+LVA+L+IQP VATL
Sbjct: 72  VDLSVGAVMAISGAVAATLTQAGWGLTPVLAASLAAGLLCGLWNGLLVAVLRIQPIVATL 131

Query: 142 ILMVAGRGVAQLITAGQIVTFNSPDLSWFGSGSLLFLPTPVIIAVLTLILFWLLTRKTAL 201
           ILMVAGRG+AQL+T GQIVTF SP L++ GSGS L +P PV+I  + L +  LL R TAL
Sbjct: 132 ILMVAGRGIAQLVTEGQIVTFTSPGLTFIGSGSFLTVPMPVVITAVLLGVTALLVRMTAL 191

Query: 202 GMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGLCAAIAGIIVAADIRGADANNAGLWLE 261
           G+ IEAVG++  ++  AGVNT ++++  YV  GLCAA+AG++VAADIRGADANNAGLWLE
Sbjct: 192 GLMIEAVGVSRLSSAGAGVNTPVVLVAVYVWCGLCAAVAGLVVAADIRGADANNAGLWLE 251

Query: 262 LDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGMNTGILLSGFPPEMNQVVKAVVVLCVL 321
           LDAILAVV+GG SL+GGRF LLLSVVGAL IQ MNTGILLSGF PE N +VKA V++ VL
Sbjct: 252 LDAILAVVVGGTSLLGGRFGLLLSVVGALTIQAMNTGILLSGFKPEFNLIVKAGVLMVVL 311

Query: 322 IVQS 325
           ++QS
Sbjct: 312 LLQS 315


Lambda     K      H
   0.327    0.142    0.416 

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: 402
Number of extensions: 15
Number of successful extensions: 1
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: 341
Length of database: 354
Length adjustment: 29
Effective length of query: 312
Effective length of database: 325
Effective search space:   101400
Effective search space used:   101400
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 Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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