GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Phaeobacter inhibens BS107

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate GFF3855 PGA1_78p00190 sn-glycerol-3-phosphate import ATP-binding protein UgbC

Query= reanno::psRCH2:GFF857
         (371 letters)



>FitnessBrowser__Phaeo:GFF3855
          Length = 361

 Score =  306 bits (784), Expect = 6e-88
 Identities = 174/362 (48%), Positives = 227/362 (62%), Gaps = 14/362 (3%)

Query: 3   SVTLRDICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDLLI 62
           SV +RD+   +    +   ++LDIE GEF+V +G SGCGKSTLL  IAGL DI+ G + I
Sbjct: 7   SVEIRDLDLHFGELQVLHQLNLDIEQGEFLVLLGSSGCGKSTLLNCIAGLLDISDGQIFI 66

Query: 63  DNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEILQ 122
             Q V    P +R +GMVFQSYALYP MTV  N++FGLK A + K EI +RV   AE+LQ
Sbjct: 67  QGQNVTWAEPSERGIGMVFQSYALYPQMTVEGNLSFGLKNARLPKAEIAKRVARAAEVLQ 126

Query: 123 LDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLHQR 182
           ++ LL+RKP  LSGGQRQRVAIGR +VR+  VFLFDEPLSNLDA LR  +R+E+ RLHQ+
Sbjct: 127 IEPLLKRKPAALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRADLRVELKRLHQQ 186

Query: 183 IRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQMNFV 242
           + +TMIYVTHDQVEAMTLAD+I ++  G I Q+  P  +Y+ P+N +VAGF+GSP MN +
Sbjct: 187 LANTMIYVTHDQVEAMTLADRIAIMKGGRIMQLSSPDEIYNRPQNLYVAGFIGSPAMNLI 246

Query: 243 EVRAISASPETVTIELP-SGYPL-TLPVDGSAVSPGDPLTLGIRPEHFVMPDE---ADFT 297
           E   I       ++ LP   Y     P  G+AV       +GIRPEH +  ++   AD T
Sbjct: 247 EGVLIDGVFHAGSLALPMQRYDYRNGPHHGAAV-------IGIRPEHILTGEQITRADAT 299

Query: 298 FHGQITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADKCHLFRENG 357
               + + E LG   L+Y T       + L +DG  RV+ G+    G    +  LF  N 
Sbjct: 300 AEVLVDLVEGLGSDTLVYAT--HGAQNLRLRMDGASRVSAGDRLRIGFDTGRASLFDPNT 357

Query: 358 EA 359
           EA
Sbjct: 358 EA 359


Lambda     K      H
   0.322    0.139    0.405 

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: 388
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: 371
Length of database: 361
Length adjustment: 30
Effective length of query: 341
Effective length of database: 331
Effective search space:   112871
Effective search space used:   112871
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 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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