GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpA in Desulfovibrio vulgaris Miyazaki F

Align Anaerobic glycerol-3-phosphate dehydrogenase subunit A1; G-3-P dehydrogenase A1; G3PDH A1; EC 1.1.5.3 (characterized)
to candidate 8500375 DvMF_1126 FAD dependent oxidoreductase (RefSeq)

Query= SwissProt::D4GYI2
         (586 letters)



>FitnessBrowser__Miya:8500375
          Length = 392

 Score =  277 bits (708), Expect = 6e-79
 Identities = 159/388 (40%), Positives = 216/388 (55%), Gaps = 11/388 (2%)

Query: 7   VLVIGGGSTGTGIARDLAMRGLDVTLVEKGNLTHGTTGRMHGLLHSGGRYAVSDQPSAKE 66
           + +IGGG T   +A DL +RG  V + E+G    G+TGR HGLLHSG RYAV D  +A+E
Sbjct: 4   IAIIGGGGTAAALAHDLILRGFSVAIYERGEFFSGSTGRHHGLLHSGARYAVHDPEAARE 63

Query: 67  CIEENRVLRRIAGHCVEMTGGLFVQRPEDSDEYFEKKLEGCRECGIPAEVLSAEEAREIE 126
           CIEEN +LRR+    +E   GLFV   ++   Y ++  + C   GIP    + E+AR +E
Sbjct: 64  CIEENMILRRLVPQAMEQNEGLFVALDDEDMAYRQRLKDACAATGIPTRDYTPEQARSME 123

Query: 127 PYLAKDIKRAIKVPDGAVDPFRLCVANAASAVEHGARIETHSEVTDVLVEGGEVVGVEVT 186
           P L   +  A++VPD   D +RL +   A+A   GA I   +EV  + V+GG V G+ + 
Sbjct: 124 PGLTDTLLAAMQVPDATFDAWRLALPFLATARAGGATIHNFTEVIGIDVQGGAVRGLRLR 183

Query: 187 HQTGTGPYVHGEPGEVEEIRADYVVNATGAWAGQIGDFAGVNVEVRPSKGVMTIMNTRQV 246
             T      HG  G      AD VVNA GAWAG++   AGV+V ++P  GV+  +  R  
Sbjct: 184 TLTED---AHGARGREWSAPADMVVNAAGAWAGKVAALAGVHVPIQPGPGVLVAIEGRVT 240

Query: 247 DTVVNRCRPKGDADIIVPHETTCILGTTDEEVEDPE--DYPEEGWEVDLMIETLSELVPM 304
           + V+NR R   + DIIVP     +LGT+    +DP+  D P E   V  M+   SE+VP 
Sbjct: 241 NMVINRMRKASEGDIIVPQRRLSVLGTSMWLTDDPDHLDIPPE--HVQRMVRLCSEMVPA 298

Query: 305 LADARTIRSFW-GVRPLYEPPGTGTEDPTDITREFFLLDHADRDDLPGMTSIVGGKLTTY 363
            ADA  IRS W   RPL          P +I+R F   DH  RD++ G+ SI+GGK  T 
Sbjct: 299 CADA-PIRSAWSAARPLI--GNADAARPQEISRTFDCYDHGTRDNVSGLLSIIGGKGMTL 355

Query: 364 RMMAEQISDHVCEKLGVDAECRTADEPL 391
           R MAE+ +D +C   G DA CRT + PL
Sbjct: 356 RAMAEKTADIICRLTGRDAPCRTRETPL 383


Lambda     K      H
   0.316    0.134    0.400 

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: 549
Number of extensions: 23
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: 586
Length of database: 392
Length adjustment: 34
Effective length of query: 552
Effective length of database: 358
Effective search space:   197616
Effective search space used:   197616
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 (21.6 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