GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ofoa in Desulfovibrio vulgaris Hildenborough

Align 2-oxoacid:ferredoxin oxidoreductase 2, subunit alpha; OFOR2; EC 1.2.7.11 (characterized)
to candidate 207415 DVU1945 pyruvate ferredoxin oxidoreductase, alpha subunit, putative

Query= SwissProt::Q9YBX7
         (642 letters)



>MicrobesOnline__882:207415
          Length = 382

 Score =  179 bits (454), Expect = 2e-49
 Identities = 126/365 (34%), Positives = 192/365 (52%), Gaps = 28/365 (7%)

Query: 234 RRGQTMMVATGNDLVAMGKIVGGLGVITYYPITPSSDEALYVEKHSYISIDGPLAEKLGY 293
           RR +  + A GN+ VA G ++ G      YPITPS++            I   +A +L  
Sbjct: 7   RRKRRELFALGNEAVAEGALLAGCTFYAGYPITPSTE------------IMEVMAARLPR 54

Query: 294 DKIAVAIVQMEDELASINAVLGAAAAGARASTTTSGPGFSLMNEAVSLAVEAEIPVVVTL 353
            +  V  +QMEDE+AS+ A +GA+ AG +A T TSGPGFSLM E +  A   E P+V+  
Sbjct: 55  MEDGV-FIQMEDEIASMGAAIGASLAGRKAMTATSGPGFSLMQEHIGYACMVEAPLVIVN 113

Query: 354 WMRAGPSTGMPTRTGQQDLLHSIFSGHGDAPKIVLASGDHVEAFYDAIKAFNWAEEFQTP 413
            MR GPSTG+PT   Q D+  + +  HGD P IVL++ +  E     + AFN+AE+++TP
Sbjct: 114 VMRGGPSTGLPTCPAQGDVQMARWGTHGDHPIIVLSASNVQECLEMTVTAFNYAEKYRTP 173

Query: 414 VIHLLDKYLASS----MVSLAREDLDPSKVPITRGKLLDNPPADYRRYEVVEDGISPRAR 469
           VI L+D+  A +    +V  A E    S+V  T       PP  ++ Y     G+     
Sbjct: 174 VILLIDEVTAHTREKIIVPHAEELEIISRVEPT------VPPEWFKPYADTVRGVPAMPA 227

Query: 470 LGSA-TMVITGLEHDEYGYATEDPVMREIMMFKRERKFKVIEERIPDEEKAVLHGDSEAS 528
           +GS   M +TGL HD  GY T+ P   + MM    R F+ I++   D +        +A 
Sbjct: 228 IGSGYRMHVTGLTHDVMGYPTQRPDEVKDMML---RLFRKIDQFYGDIQLTDSFALEDAE 284

Query: 529 VALVSFGSTKQPILEALEMLRDEGVRARFAQVRLLYPFPGRLVEEMLEGVEKVIMVEQNL 588
           VA++++GS  +    A+E  R+ G +A    ++ L+PFP   VE +      +++ E N 
Sbjct: 285 VAVIAYGSVARSAHLAVEQARERGAKAGLLTLKTLFPFPRPAVETLARRCSILVVPEMN- 343

Query: 589 LGQLA 593
           +GQ++
Sbjct: 344 MGQMS 348


Lambda     K      H
   0.318    0.135    0.380 

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: 500
Number of extensions: 22
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: 642
Length of database: 382
Length adjustment: 34
Effective length of query: 608
Effective length of database: 348
Effective search space:   211584
Effective search space used:   211584
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: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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