GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Marinobacter adhaerens HP15

Align spermidine/putrescine ABC transporter, ATP-binding protein PotA; EC 3.6.3.31 (characterized)
to candidate GFF3011 HP15_2955 ATP-binding component of ABC transporter

Query= CharProtDB::CH_024626
         (378 letters)



>FitnessBrowser__Marino:GFF3011
          Length = 372

 Score =  246 bits (627), Expect = 1e-69
 Identities = 143/361 (39%), Positives = 218/361 (60%), Gaps = 19/361 (5%)

Query: 18  VQLAGIRKCFDG--KEVIPQLDLTINNGEFLTLLGPSGCGKTTVLRLIAGLETVDSGRIM 75
           ++L  IRK + G  +E +  +D+ I +GEFL L+GPSGCGK+T++  IAGLET+  G I+
Sbjct: 4   LELRSIRKTYPGVAEETLKGIDIDIASGEFLILVGPSGCGKSTLMNTIAGLETITDGSIV 63

Query: 76  LDNEDITHVPAENRYVNTVFQSYALFPHMTVFENVAFGLRMQKTPAAEITPRVMEALRMV 135
           LD +DI+ +  ++R +  VFQSYAL+P M+V EN+AFGL+++  P  EI   V     ++
Sbjct: 64  LDGKDISTMEPKDRDIAMVFQSYALYPTMSVRENIAFGLKIRGLPKHEIDQEVERVADLL 123

Query: 136 QLETFAQRKPHQLSGGQQQRVAIARAVVNKPRLLLLDESLSALDYKLRKQMQNELKALQR 195
           Q+     +KP  LSGGQQQRVA+ RA+  +PR+ L DE LS LD KLR +M+ E+K L +
Sbjct: 124 QISPLMNKKPANLSGGQQQRVAMGRALARRPRIYLFDEPLSNLDAKLRVEMRTEIKKLHQ 183

Query: 196 KLGITFVFVTHDQEEALTMSDRIVVMRDGRIEQDGTPREIYEEPKNLFVAGFIGEINMFN 255
           +L  T V+VTHDQ EA+T++DRI V++DG ++Q GTP+E+Y+ P+NLFVAGF+G   M  
Sbjct: 184 RLKTTIVYVTHDQIEAMTLADRIAVLKDGELQQLGTPKEVYDRPENLFVAGFMGSPAMSF 243

Query: 256 ATVIERLDEQRVRANV---EGRECNIYVN--FAVEPGQKLHVLLRPEDLRVEEINDDNHA 310
             V     E  ++A V   +GR   + V    A   G+K+ + +RPE   + +  D  + 
Sbjct: 244 VPVTVEQGEGGLQAEVRGNDGRSVKLPVPEFLADRVGKKVILGIRPE--HITQPQDQKND 301

Query: 311 EGLIGYVRERNYKGMTLESVVELENGKMVMVSEFFNEDDPDFDHSLDQKMAINWVESWEV 370
           + L+        KG   E  +E+       V      +D +    +D +  + W E+ E+
Sbjct: 302 QTLVA-------KG---EFTIEVTEPTGPDVIALIQLNDTNVHCRIDPEHPVTWGETAEL 351

Query: 371 V 371
           +
Sbjct: 352 M 352


Lambda     K      H
   0.319    0.136    0.385 

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: 345
Number of extensions: 13
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: 378
Length of database: 372
Length adjustment: 30
Effective length of query: 348
Effective length of database: 342
Effective search space:   119016
Effective search space used:   119016
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 (21.7 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