GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lldF in Desulfovibrio vulgaris Miyazaki F

Align L-lactate dehydrogenase iron-sulfur cluster-binding protein LldF (characterized, see rationale)
to candidate 8499630 DvMF_0396 iron-sulfur cluster binding protein (RefSeq)

Query= uniprot:Q8EGS5
         (464 letters)



>FitnessBrowser__Miya:8499630
          Length = 475

 Score =  282 bits (721), Expect = 2e-80
 Identities = 163/393 (41%), Positives = 226/393 (57%), Gaps = 16/393 (4%)

Query: 10  MGSQVHAYKADI---FCRDETRVDWHSKALWLLREKRDRAAGSLPEWEQLRQLGSEIKLH 66
           MGSQ   + A++       + R ++ S AL  L +KR        E E++R      K  
Sbjct: 1   MGSQHLDFTANVTEALADRQLRANFKS-ALTGLMKKRVAVLPDAAERERMRDDAEAAKRK 59

Query: 67  TLTNLAQYLETFEQNCLANGIKVHWAKDGAEHNRIVHEILASHKVKKLVKSKSMLTEECH 126
            L  L + LE  E+ C  NGI VHWA+  AE N I+ +I+ SH   +LVK KSM++EE H
Sbjct: 60  ALAKLPELLERLERKCTENGIIVHWAETTAEANEIILDIMRSHDATRLVKGKSMVSEEMH 119

Query: 127 LNPYLEQRGIEVIDTDLGERIIQLAKMPPSHIVVPAIHMKKEEVGDLFHDKLGTKAGESD 186
           LN +LE  GIE ++TDLGE IIQL   PPSHI+VPA+H  +++VG +F D L        
Sbjct: 120 LNHFLETHGIEALETDLGEFIIQLNHEPPSHIIVPAVHKNRQQVGRIFADNLQGIPYTDV 179

Query: 187 PLYLTRAARAHLREQFLSADAAMTGVNMAIADKGAVVVCTNEGNADMGANLPKLQLHSMG 246
              L   AR  LRE+F +    ++GVN A+A+ G +V+  NEGN  M   +P + +  MG
Sbjct: 180 VEELNAIARKTLREKFRTGHVGLSGVNFAVAETGTLVLVENEGNGRMCTTVPPVHVAVMG 239

Query: 247 IDKVVPDIDSAAVLLRTLARNATGQPVTTYSAFYRGPQVDG------EMHVIIVDNGRTE 300
           ++KVV  +     LLR L  +ATGQ VTTY      P+ DG      E+H++I+DNGR+ 
Sbjct: 240 LEKVVESLSDLPPLLRLLTASATGQLVTTYVNCITSPRKDGERDGPKEIHLVILDNGRSR 299

Query: 301 MMKDKILAESLKCIRCGGCLNTCPVYRRSGGYSYNYTIPGPIGIAVGATHD---NTNSIA 357
           M+ D  L  +L+CIRCG CLN CPVY R GG++Y    PGPIG  +    D   +   +A
Sbjct: 300 MLADAQLRRTLQCIRCGTCLNHCPVYIRIGGHAYGSVYPGPIGKILTPQIDGLADKGVLA 359

Query: 358 WACTLCGSCTYVCPTKVPLDKIIHHHRRLKAEA 390
            A +LC +C  VCP ++P+  II   RR++ EA
Sbjct: 360 TASSLCNACEEVCPVRIPIPGII---RRMRTEA 389


Lambda     K      H
   0.320    0.134    0.413 

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: 512
Number of extensions: 23
Number of successful extensions: 5
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: 464
Length of database: 475
Length adjustment: 33
Effective length of query: 431
Effective length of database: 442
Effective search space:   190502
Effective search space used:   190502
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 (21.8 bits)
S2: 51 (24.3 bits)

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

Links

Downloads

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:

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