Alignments for a candidate for glpD in Cereibacter sphaeroides ATCC 17029

GapMind for catabolism of small carbon sources

Alignments for a candidate for glpD in Cereibacter sphaeroides ATCC 17029

Align Glycerol-3-phosphate dehydrogenase; EC 1.1.5.3 (characterized, see rationale)
to candidate WP_011840947.1 RSPH17029_RS06725 glycerol-3-phosphate dehydrogenase

Query= uniprot:Q92LM5
         (503 letters)



>NCBI__GCF_000015985.1:WP_011840947.1
          Length = 539

 Score =  564 bits (1454), Expect = e-165
 Identities = 297/515 (57%), Positives = 348/515 (67%), Gaps = 23/515 (4%)

Query: 8   DVFVIGGGINGCGIARDAAGRGYSVALAEMSDFASGTSSGSTKLIHGGLRYLEHYEFRLV 67
           D+F+IGGGINGCGIARDAAGRG SV LAEM D A  TSS STKL HGGLRYLE++EFRLV
Sbjct: 19  DLFIIGGGINGCGIARDAAGRGLSVTLAEMGDLAQATSSASTKLFHGGLRYLEYFEFRLV 78

Query: 68  REALMEREVLWAMAPHVIWPMRFVLPFHKG---------------------GPRPAWLIR 106
           REAL ERE L    PH+ WPMRFVLP+                        G RPAWLIR
Sbjct: 79  REALEERETLLVAMPHISWPMRFVLPWQPEMRFAGDTPTAQLLGRLMPWARGRRPAWLIR 138

Query: 107 LGLFLYDHIGGRKLLPATKTLDMTRDPAGAPLKGLFTKAFEYSDGWVDDARLVVLNARDA 166
           L L  YD +GGRK+LP  +++D+TRDPAG  L+  FTK +EYSD WV+D+RLVVLNARDA
Sbjct: 139 LALETYDRLGGRKILPPARSVDLTRDPAGRALQPRFTKGWEYSDCWVEDSRLVVLNARDA 198

Query: 167 ADRGARIMARTRVVSARREGGRWAIEIESTETGARETMRARMLVNAAGPWVDRVLSEAVG 226
             RGA I+ RT+VV A R G  W +  E      R+  R R LVNA GPWV R++ E + 
Sbjct: 199 EIRGATILTRTKVVGAERRGDLWHVTTEGAR--GRQVHRVRALVNAGGPWVARIIRETLA 256

Query: 227 NNDVRNVRLVQGSHIVVKKKFDDPRAYFFQNPDGRIMFAIPYQDEFTLIGTTDRDFTGNP 286
                 VRLV+GSHIV K+ FD  R YFFQ  DGRI+FAIPY+ +FTLIGTTD+D  G P
Sbjct: 257 LPTTEGVRLVRGSHIVTKRLFDHDRCYFFQGTDGRIIFAIPYETDFTLIGTTDQDHRGAP 316

Query: 287 ADVRISDAEIDYLCRAASEYFSDPVGREDIVWTYSAVRPLFDDGASKAQEATRDYVLRVE 346
            + R +  E DYLC  AS+YF  PV REDIVWTYS VRPL DDGA  A  ATRDYVL ++
Sbjct: 317 DEARCTPEEQDYLCAFASDYFRKPVTREDIVWTYSGVRPLHDDGARSATAATRDYVLSLD 376

Query: 347 NGDAPLLNVFGGKLTTYRRLAESALEKIGETIGEKGRKWTAVSHLPGGDFPAAGYDDEVA 406
           +  APLLNVFGGK+TTYRRLAESA+ K+ E   +    WTA   LPGGDFP  G      
Sbjct: 377 SRGAPLLNVFGGKITTYRRLAESAMAKLAEHFPQARGAWTARVPLPGGDFPWDGAPALAE 436

Query: 407 KLRTRYPFLTASHARRLVRLYGTRAAQLLGNAASEADLGKHFGADLYAAEVDWLIVQEWA 466
            LR  YPFLT   A RLVR YGT A  LLG A S  DLG+ FGA L  AEV WL+ +E+A
Sbjct: 437 GLRRDYPFLTERWAMRLVRAYGTDARNLLGPARSALDLGRDFGATLTEAEVRWLMDREYA 496

Query: 467 LRAEDVLWRRTKLGLKFSRAQTAELEEYMRGAVNA 501
            RAEDV+WRR+KLGL+ +  + A L+ +M+ A  A
Sbjct: 497 ERAEDVVWRRSKLGLRLTPEEIAALDGWMKDAGGA 531


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: 908
Number of extensions: 36
Number of successful extensions: 4
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: 539
Length adjustment: 35
Effective length of query: 468
Effective length of database: 504
Effective search space:   235872
Effective search space used:   235872
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 Apr 10 2024. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

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 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