GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Sphingomonas koreensis DSMZ 15582

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate Ga0059261_2632 Ga0059261_2632 FAD binding domain

Query= reanno::Smeli:SMc00833
         (405 letters)



>FitnessBrowser__Korea:Ga0059261_2632
          Length = 364

 Score =  277 bits (709), Expect = 3e-79
 Identities = 166/372 (44%), Positives = 207/372 (55%), Gaps = 28/372 (7%)

Query: 27  LAVVGGGTRAGLGNPVRADRTLSTRRLSGIVTYDPAEMTMSALAGTPVAEVEAALHAKGQ 86
           L + GGG++  +G P  A + +  R  SGIV YDP E+ ++  AGTP+A++EA +  +GQ
Sbjct: 20  LRLRGGGSKDAIGAPCDA-QVVDMRGFSGIVDYDPPELVLTVGAGTPLAQIEALVVGEGQ 78

Query: 87  MLSFEPMDHRPIFATTGEPTIGGVFAANVSGPRRYVAGAARDSLLGVRFVNGRGEPIKAG 146
           ML+F+P DH  +    G  TIGGV AA V+GP R   G ARD LLG   V+GRGE   AG
Sbjct: 79  MLAFDPFDHGAMLGNDGGATIGGVVAAGVAGPARLSRGGARDHLLGFTAVSGRGERFVAG 138

Query: 147 GRVMKNVTGLDLVKLMAGSYGTLGILTEVTFKVLPLPPAAATVVVSGLNDAEAAAVMAEA 206
            +V+KNVTG DL KLMAGS+G L  LTEVT KVLP P    T+ + GL+ A A A MA A
Sbjct: 139 AKVVKNVTGYDLPKLMAGSWGRLAALTEVTLKVLPAPRTRLTLAMRGLDAAGAVAAMARA 198

Query: 207 MAQPVEVSGASHLPESVRSRFLDGALPDGAATVLRLEGLAASVAIRAEKLGEKLSRFGRI 266
           +    EV+ A+HLP+              A T LRL+G A SVA RA  L E    F  I
Sbjct: 199 LGSAAEVTAAAHLPD----------WRGEAVTALRLDGFAESVAARAAMLPE----FDAI 244

Query: 267 SQLDEAQTRTLWAEIRDVKPYADGTRRPLWRISVAPSAGHQLVAALRLQTGVDAFYDWQG 326
              D      LW  +RD  P       PLWR+ VAP     ++AAL          DW G
Sbjct: 245 EDAD-----ALWRAVRDASPLP--REWPLWRLIVAPGKAPGVIAAL---PDAQWLLDWAG 294

Query: 327 GLVWLRMEADPEAELLRRYIGAVGGGHAALLRAGEEARGRIPAFEPQPPAVARLSERIRA 386
           GL+WL  +A P A    R      GGHA L RA E  R  +PA  PQP A+A +  R+R 
Sbjct: 295 GLIWLTSDAGPVA---IRTAAEAAGGHATLWRASEAMRRAVPALHPQPGALAAIEARVRR 351

Query: 387 QFDPSGIFNPGR 398
            FDP G+F  GR
Sbjct: 352 AFDPGGVFETGR 363


Lambda     K      H
   0.318    0.134    0.387 

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: 498
Number of extensions: 28
Number of successful extensions: 6
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: 405
Length of database: 364
Length adjustment: 30
Effective length of query: 375
Effective length of database: 334
Effective search space:   125250
Effective search space used:   125250
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