Alignments for a candidate for glpD in Brucella inopinata BO1

GapMind for catabolism of small carbon sources

Alignments for a candidate for glpD in Brucella inopinata BO1

Align Glycerol-3-phosphate dehydrogenase; EC 1.1.5.3 (characterized, see rationale)
to candidate WP_008506738.1 BIBO1_RS10825 glycerol-3-phosphate dehydrogenase

Query= uniprot:Q92LM5
         (503 letters)



>NCBI__GCF_000182725.1:WP_008506738.1
          Length = 503

 Score =  704 bits (1816), Expect = 0.0
 Identities = 342/503 (67%), Positives = 406/503 (80%), Gaps = 2/503 (0%)

Query: 1   MSEQTIFDVFVIGGGINGCGIARDAAGRGYSVALAEMSDFASGTSSGSTKLIHGGLRYLE 60
           M ++  FD+F+IGGGINGCGIARDA GRG++V LAEM+D ASGTSS +TKLIHGGLRYLE
Sbjct: 1   MVQEKQFDIFIIGGGINGCGIARDAVGRGFTVGLAEMNDLASGTSSRATKLIHGGLRYLE 60

Query: 61  HYEFRLVREALMEREVLWAMAPHVIWPMRFVLPFHKGGPRPAWLIRLGLFLYDHIGGRKL 120
           HYEFRLVREALMEREVLWA APH+I PMRFVLP+HKGG RPAWL+RLGLFLYDH+GGRK 
Sbjct: 61  HYEFRLVREALMEREVLWANAPHIIHPMRFVLPYHKGGLRPAWLLRLGLFLYDHLGGRKK 120

Query: 121 LPATKTLDMTRDPAGAPLKGLFTKAFEYSDGWVDDARLVVLNARDAADRGARIMARTRVV 180
           LPAT+TL+M  D AG PLK LFTKAFEYSD WVDDAR V L ARDAADRGA I  RT VV
Sbjct: 121 LPATRTLNMRTDKAGEPLKPLFTKAFEYSDCWVDDARFVALTARDAADRGAMIATRTSVV 180

Query: 181 SARREGGRWAIEIESTETGARETMRARMLVNAAGPWVDRVLSEAVGNNDVRNVRLVQGSH 240
           +A R+G  W I +E T TG RE + AR+LVNAAGPW D+VL    G+  + N+RLVQGSH
Sbjct: 181 AASRDGQGWTITLEDTGTGRRENVHARLLVNAAGPWADKVLQGVEGDRQLHNIRLVQGSH 240

Query: 241 IVVKKKFDDPRAYFFQNPDGRIMFAIPYQDEFTLIGTTDRDFTGNPADVRISDAEIDYLC 300
           IVV++KF DPRAYFFQN DGRI+FAIPY+D+FTLIGTTD+D+ G+PA V I+D+E +YLC
Sbjct: 241 IVVRRKFSDPRAYFFQNNDGRIIFAIPYEDDFTLIGTTDQDYKGDPAKVAITDSETEYLC 300

Query: 301 RAASEYFSDPVGREDIVWTYSAVRPLFDDGASKAQEATRDYVLRVE--NGDAPLLNVFGG 358
           +AASEYF +PV REDIVWTYS VRPL+DDGASKAQEATRDYVL+ +  +G APL+NVFGG
Sbjct: 301 QAASEYFREPVRREDIVWTYSGVRPLYDDGASKAQEATRDYVLKEDAPDGLAPLINVFGG 360

Query: 359 KLTTYRRLAESALEKIGETIGEKGRKWTAVSHLPGGDFPAAGYDDEVAKLRTRYPFLTAS 418
           KLTT R+LAE  L+KI   +G KG  WT  + LPGGDF    ++ E+ KL   YPFL A 
Sbjct: 361 KLTTARKLAEHMLQKIEHRLGRKGAPWTHAAPLPGGDFEDVAFETELKKLEAAYPFLDAR 420

Query: 419 HARRLVRLYGTRAAQLLGNAASEADLGKHFGADLYAAEVDWLIVQEWALRAEDVLWRRTK 478
           HARRL RLYGT+A +LLG A+S  DLG+HFG+DLY AEV +L+  EWA  AED+LWRRTK
Sbjct: 421 HARRLFRLYGTQAYKLLGQASSLGDLGRHFGSDLYEAEVRYLVENEWARSAEDILWRRTK 480

Query: 479 LGLKFSRAQTAELEEYMRGAVNA 501
           LGL+ + A+ A ++ ++  A+ A
Sbjct: 481 LGLRLTAAEVAAVQGFVEPAIAA 503


Lambda     K      H
   0.321    0.137    0.417 

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: 827
Number of extensions: 25
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: 503
Length of database: 503
Length adjustment: 34
Effective length of query: 469
Effective length of database: 469
Effective search space:   219961
Effective search space used:   219961
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: 52 (24.6 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources