GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Synechococcus elongatus PCC 7942

Align ABC transporter for D-Mannitol, D-Mannose, and D-Sorbitol, ATPase component (characterized)
to candidate Synpcc7942_0960 Synpcc7942_0960 ATPase

Query= reanno::WCS417:GFF2490
         (367 letters)



>FitnessBrowser__SynE:Synpcc7942_0960
          Length = 417

 Score =  286 bits (732), Expect = 7e-82
 Identities = 165/370 (44%), Positives = 218/370 (58%), Gaps = 27/370 (7%)

Query: 18  IIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSEGTIELDGRDITEVTPAKRDL 77
           ++ GI+LE+ D EF+V VGPSGCGKSTLLRL+AGLE  S G I++  R +  +    RD+
Sbjct: 49  VLNGINLEIADGEFMVVVGPSGCGKSTLLRLLAGLETPSRGLIKVGDRRVDRLPAKARDI 108

Query: 78  AMVFQTYALYPHMSVRKNMSFALDLAG---------------VDKKL---------VESK 113
           AMVFQ+YALYPH+SV  N++F L   G               + K L         ++ +
Sbjct: 109 AMVFQSYALYPHLSVYDNLAFGLRRQGDRPWWQQQLALATRSLPKSLQYEPEQEARIKRR 168

Query: 114 VSEAARILELGPLLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMR 173
           V E A +L+L  LL+R+PKQLSGGQ+QRVA+GRAI RNP++FL DEPLSNLDA LR + R
Sbjct: 169 VREVATMLQLDTLLDRQPKQLSGGQKQRVALGRAIARNPQVFLMDEPLSNLDAKLRAETR 228

Query: 174 LELARLHKELQATMIYVTHDQVEAMTLADKVVVLNSGRIEQVGSPLELYHQPANLFVAGF 233
            ++  L ++L  T +YVTHDQ EAMT+ D++ VLN G ++QV SPLE+Y +PAN FVA F
Sbjct: 229 AQIVSLQRQLGVTTLYVTHDQTEAMTMGDRIAVLNRGHLQQVASPLEIYDRPANRFVAQF 288

Query: 234 LGTPKMGFLKGKVTRVESQSCEVQLDAGTLINLPLSGATLSVGSAVTLGIRPEHLEIASP 293
           +G+P M  +   VT         +    TL         L  G  V LGIRPEHLE+ + 
Sbjct: 289 IGSPPMNLI--PVTVRAPLQLTTENFRCTLPEAWEPVLRLYDGQTVELGIRPEHLEVGAA 346

Query: 294 GQTTLTVTADVGERLGSDTF-CHVITANGEPLTMRIRGDMASQYGETLHLHLDPAHCHLF 352
               L +T    E LGSDTF    +  +G  +  R+      Q G+ L L   P   HLF
Sbjct: 347 ASKNLLITVTGVEALGSDTFIAGELKESGIAVQARLAPQQCWQMGDRLWLTFKPDQIHLF 406

Query: 353 DTDGVAVARP 362
           D +     RP
Sbjct: 407 DLETGKAIRP 416


Lambda     K      H
   0.319    0.136    0.384 

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: 409
Number of extensions: 16
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: 367
Length of database: 417
Length adjustment: 31
Effective length of query: 336
Effective length of database: 386
Effective search space:   129696
Effective search space used:   129696
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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:

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