GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lldF in Azospirillum brasilense Sp245

Align L-lactate dehydrogenase iron-sulfur cluster-binding protein LldF (characterized, see rationale)
to candidate AZOBR_RS25110 AZOBR_RS25110 (Fe-S)-binding protein

Query= uniprot:Q8EGS5
         (464 letters)



>FitnessBrowser__azobra:AZOBR_RS25110
          Length = 474

 Score =  286 bits (731), Expect = 1e-81
 Identities = 145/361 (40%), Positives = 216/361 (59%), Gaps = 12/361 (3%)

Query: 39  LREKRDRAAGSLPEWEQLRQLGSEIKLHTLTNLAQYLETFEQNCLANGIKVHWAKDGAEH 98
           L  KR        EW  +R LG+ ++L  L+ L + LE  E NC  NGI+VHWA    E 
Sbjct: 32  LMSKRAVQFADTAEWNGVRTLGASVRLRALSKLPELLEKLEANCTKNGIQVHWASTTDEA 91

Query: 99  NRIVHEILASHKVKKLVKSKSMLTEECHLNPYLEQRGIEVIDTDLGERIIQLAKMPPSHI 158
           N IV  I+     K +VK KSM++EE HLN +LE+ GIE +++DLGE I+QL +  PSHI
Sbjct: 92  NAIVLSIMQRVNAKLVVKGKSMVSEEMHLNAFLEKHGIESLESDLGEYIVQLDEAMPSHI 151

Query: 159 VVPAIHMKKEEVGDLFHDKLGTKAGESDPLYLTRAARAHLREQFLSADAAMTGVNMAIAD 218
           ++PAIHM  +++  LF  K+       D   LT  AR  LR++F +AD  ++GVNMA+A+
Sbjct: 152 IMPAIHMNTKQIAHLFKQKIKEAEYTEDVAQLTDLARRVLRKKFATADVGISGVNMAVAE 211

Query: 219 KGAVVVCTNEGNADMGANLPKLQLHSMGIDKVVPDIDSAAVLLRTLARNATGQPVTTYSA 278
            G + +  NEGN  M   +P + +  MG++KVV  ++    ++  L R+AT QP+TTY  
Sbjct: 212 TGTLCLVENEGNGRMSTTVPPVHIAVMGLEKVVEKLEDVPPVISLLTRSATAQPITTYVN 271

Query: 279 FYRGPQVDG------EMHVIIVDNGRTEMMKDKILAESLKCIRCGGCLNTCPVYRRSGGY 332
               P+ +G      E+H++I+DNGR+ +  D+ L  +L+CIRCG C+N CPVY + GG+
Sbjct: 272 MISSPRKEGEKDGPNEIHLVILDNGRSGIYADEELRNTLRCIRCGACMNHCPVYTKVGGH 331

Query: 333 SYNYTIPGPIGIAVGAT---HDNTNSIAWACTLCGSCTYVCPTKVPLDKIIHHHRRLKAE 389
           +Y    PGPIG  +       +    +  ACT+C +C  +CP K+P+ +I+    RL++E
Sbjct: 332 AYQAPYPGPIGSILMPQVEGLEKRGELPHACTMCNACVEICPVKIPIVEIM---GRLRSE 388

Query: 390 A 390
           A
Sbjct: 389 A 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: 510
Number of extensions: 21
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 464
Length of database: 474
Length adjustment: 33
Effective length of query: 431
Effective length of database: 441
Effective search space:   190071
Effective search space used:   190071
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