GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Phaeobacter inhibens BS107

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate GFF3855 PGA1_78p00190 sn-glycerol-3-phosphate import ATP-binding protein UgbC

Query= reanno::WCS417:GFF4321
         (386 letters)



>FitnessBrowser__Phaeo:GFF3855
          Length = 361

 Score =  304 bits (779), Expect = 2e-87
 Identities = 170/366 (46%), Positives = 229/366 (62%), Gaps = 14/366 (3%)

Query: 3   TLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGGAI 62
           ++E+R+++  +G      L  + L I++GEFL+L+G SGCGKSTL+NCIAGL  I+ G I
Sbjct: 7   SVEIRDLDLHFGE--LQVLHQLNLDIEQGEFLVLLGSSGCGKSTLLNCIAGLLDISDGQI 64

Query: 63  MIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVAKL 122
            I  Q+V+   P +R I MVFQSYALYP M+V  N+ FGLK  ++P+A+I   VAR A++
Sbjct: 65  FIQGQNVTWAEPSERGIGMVFQSYALYPQMTVEGNLSFGLKNARLPKAEIAKRVARAAEV 124

Query: 123 LQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLMH 182
           LQIE LL RKP  LSGGQ+QRVA+GRAL R   ++LFDEPLSNLDAKLR ++R E+K +H
Sbjct: 125 LQIEPLLKRKPAALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRADLRVELKRLH 184

Query: 183 QRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPPMN 242
           Q+L  T +YVTHDQ+EAMTL D++A+MK G I Q  +P EIYN P N +VA FIGSP MN
Sbjct: 185 QQLANTMIYVTHDQVEAMTLADRIAIMKGGRIMQLSSPDEIYNRPQNLYVAGFIGSPAMN 244

Query: 243 FVPLRLQRKDGRLV-ALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDSA 301
            +       +G L+  +  +G     +       G      ++G+RPE I+   GE  + 
Sbjct: 245 LI-------EGVLIDGVFHAGSLALPMQRYDYRNGPHHGAAVIGIRPEHIL--TGEQITR 295

Query: 302 SSIRAEVQV--TEPTGPDTLVFVQLNDTKVCCRLAPDVAPQVGETLTLQFDPSKVLLFDA 359
           +   AEV V   E  G DTLV+       +  R+        G+ L + FD  +  LFD 
Sbjct: 296 ADATAEVLVDLVEGLGSDTLVYATHGAQNLRLRMDGASRVSAGDRLRIGFDTGRASLFDP 355

Query: 360 NTGERL 365
           NT  RL
Sbjct: 356 NTEARL 361


Lambda     K      H
   0.318    0.135    0.382 

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: 378
Number of extensions: 14
Number of successful extensions: 2
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: 386
Length of database: 361
Length adjustment: 30
Effective length of query: 356
Effective length of database: 331
Effective search space:   117836
Effective search space used:   117836
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 (21.7 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