GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Rhodobacter johrii JA192

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate WP_069332029.1 C8J29_RS20170 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Smeli:SM_b21216
         (360 letters)



>NCBI__GCF_003046325.1:WP_069332029.1
          Length = 359

 Score =  345 bits (884), Expect = 1e-99
 Identities = 185/362 (51%), Positives = 244/362 (67%), Gaps = 12/362 (3%)

Query: 1   MSALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDI 60
           M+ + ++ I KRYG +E + G+D+ +E GEF+  +G SGCGKST+L +IAGL + SGG +
Sbjct: 1   MARISLQKIVKRYGGMEAIHGVDLEVEDGEFVAFVGPSGCGKSTMLRMIAGLEDISGGHM 60

Query: 61  LIGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARL 120
            IG+R V  + PK RD+AMVFQ YALYP+++V  NIGFGL+MR  P     K V + AR+
Sbjct: 61  RIGDRLVNDIEPKGRDVAMVFQDYALYPHMTVRDNIGFGLKMRGEPAETIRKKVEEAARI 120

Query: 121 LQIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLH 180
           LQ+E+LLDR+P QLSGGQRQRVA+GRA+VR P+VFLFDEPLSNLDAKLR+EMRT++KRLH
Sbjct: 121 LQLEDLLDRRPGQLSGGQRQRVAMGRAIVRKPKVFLFDEPLSNLDAKLRVEMRTQIKRLH 180

Query: 181 QMLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMN 240
           +MLRTT +YVTHDQ+EAMTLA R+ V+R G I Q   P E+Y+RP+  +VA F+GSP MN
Sbjct: 181 RMLRTTTIYVTHDQVEAMTLADRVVVLRKGSIIQHGRPLELYERPSCRFVAEFIGSPQMN 240

Query: 241 ILDAEMTAN--GLKIE---GCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEAQR 295
           IL   + ++  G  IE   G   +  LP         G  V VG+RPE L   A  EA  
Sbjct: 241 ILPGRVASSDRGTVIEVGGGAISLSHLPVP------VGTAVDVGLRPEHLEPCAPEEAD- 293

Query: 296 LTASVEVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGR 355
             A V+V+E  G + +    +G + IT  +P   A  +G A    FD   LHLFD  +G+
Sbjct: 294 FVAEVDVLEELGSDTLAICLMGEREITVRVPADRARSLGRAQPLRFDRQNLHLFDAANGQ 353

Query: 356 SL 357
            +
Sbjct: 354 RI 355


Lambda     K      H
   0.320    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: 377
Number of extensions: 20
Number of successful extensions: 3
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: 360
Length of database: 359
Length adjustment: 29
Effective length of query: 331
Effective length of database: 330
Effective search space:   109230
Effective search space used:   109230
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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