GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Desulfovibrio vulgaris Miyazaki F

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate 8501344 DvMF_2077 FAD-dependent pyridine nucleotide-disulphide oxidoreductase (RefSeq)

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Miya:8501344
          Length = 602

 Score =  195 bits (495), Expect = 3e-54
 Identities = 128/336 (38%), Positives = 187/336 (55%), Gaps = 45/336 (13%)

Query: 2   VEVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPG--DVHG 59
           ++V  + +++LG+GPAG SAA+Y  R+ +K +++     GGQ+T T  V+N+PG  D+ G
Sbjct: 265 LDVVETDMVVLGAGPAGLSAAIYGERSGMKTVVLDKSVVGGQVTVTPVVENYPGFTDIAG 324

Query: 60  LTGPALMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARY 119
           L    L+E +  HA ++ T    + ++ V    K   +  + A Y C AL+ ATGA  R 
Sbjct: 325 LK---LVEVLSAHARQYATVREGETVHEVKIG-KLIEVYTNRAVYLCKALVFATGAQWRK 380

Query: 120 LGLPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRE 179
           L  P E  F G+GVS CA+CDGF YR K VA++GGGN+A+ +AL+L N+ + VT+IHRR+
Sbjct: 381 LDAPGEGRFYGRGVSYCASCDGFMYRGKRVAMIGGGNSALTDALHLKNLGADVTIIHRRD 440

Query: 180 TFRAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMG---------------------- 217
           +FRAEK L D L     EG I +  +  ++E+LGD +                       
Sbjct: 441 SFRAEKALQDSLE---REG-IAVIWDTVVEEILGDTVAPVREGDGGDGKDAAPGTAPAEP 496

Query: 218 ----VTGARLKN-NDGSFDELKVDGVFIAIGHTPNTSLFE--GQLTLKDGYLVVQGGRDG 270
               V G R++N    +  EL  DGVF+AIGH PN+      G +  KDG + V      
Sbjct: 497 DTGVVRGIRVRNVKTDAVSELPFDGVFVAIGHIPNSEQAAELGVVLEKDGSIKVD----- 551

Query: 271 NATATSVEGIFAAGDVADHVYRQAITSAGAGCMAAL 306
               T++  I+AAGDV   V RQ +T+ G+G  AAL
Sbjct: 552 RHMRTNIPRIYAAGDVTGGV-RQIVTAVGSGATAAL 586


Lambda     K      H
   0.318    0.135    0.386 

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: 473
Number of extensions: 28
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: 320
Length of database: 602
Length adjustment: 32
Effective length of query: 288
Effective length of database: 570
Effective search space:   164160
Effective search space used:   164160
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: 51 (24.3 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