GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Acidovorax sp. GW101-3H11

Align Isovaleryl-CoA dehydrogenase, mitochondrial; IVD; Isovaleryl-CoA dehydrogenase 2; St-IVD2; EC 1.3.8.4 (characterized)
to candidate Ac3H11_1933 Acyl-CoA dehydrogenase, short-chain specific (EC 1.3.99.2)

Query= SwissProt::Q9FS87
         (412 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1933
          Length = 386

 Score =  253 bits (647), Expect = 5e-72
 Identities = 145/379 (38%), Positives = 214/379 (56%), Gaps = 8/379 (2%)

Query: 33  LFDDTQKQFKESVAQFAQENIAPHAEKIDRTNYFPQDVNLWKLMGNFNLLGITVPEEYGG 92
           LF    + F +S  +F ++ + PH    +   Y  ++V  W   G    L +++PEEYGG
Sbjct: 6   LFQPEHQAFADSFRRFIEKEVTPHHADWEDQGYVAREV--WSQAGANGFLCMSLPEEYGG 63

Query: 93  LGLGYLYHCIAMEEISRASGSVGLSYGAHTNLCINQLVRNGTHEQKQKYLPKLISGEHVG 152
            G   LY    MEE++RA G+ G+ +G H+ +    ++  GT EQK+KYLP++ SG  VG
Sbjct: 64  AGADKLYSVAQMEELARA-GTTGIGFGLHSEIVAPYILHYGTEEQKRKYLPQMASGAVVG 122

Query: 153 ALAMSEPNAGSDVVSMKCKADRVEGG--YVLNGNKMWCTNGPTAQTLVVYAKTDVTAGSK 210
           A+AMSEP AGSD+  +K  A +   G  YVLNG+K + TNG  A  ++V AKTD  AG+K
Sbjct: 123 AIAMSEPAAGSDLQGIKTTAIKSADGSHYVLNGSKTFITNGWHADLVIVVAKTDPAAGAK 182

Query: 211 GITAFIIEKGMTGFSTAQKLDKLGMRGSDTCELVFENCFVPEENVLG---QVGRGVYVLM 267
           G +  ++E+GM GF   Q+L KLGM+  DT EL F +  VP EN+LG     GRG   LM
Sbjct: 183 GTSLLLVERGMPGFEKGQRLKKLGMKAQDTSELFFNDVKVPAENLLGGPAMEGRGFICLM 242

Query: 268 SGLDLERLVLASGPVGIMQACLDVVLPYVKQREQFGRPIGEFQFVQGKVADMYTSMQSSR 327
             L  ERL +A   V   QA +D  L YVK+R+ FG+P+  FQ  +  +A++ T +Q +R
Sbjct: 243 EQLPWERLQIAITAVAAAQAAIDWTLDYVKERKVFGQPVASFQNTRYTLAELQTEVQVAR 302

Query: 328 SYLYSVARECDSGTINTKDCAGVILSAAERATQVALQAIQCLGGNGYVNEYPTGRFLRDA 387
            ++           ++T+  +       +   +V  + +Q  GG GY+ EYP  R   DA
Sbjct: 303 VFVDKCCELIARDQLDTQTASMAKYWTTDLQCKVMDECVQMFGGYGYMWEYPITRAYADA 362

Query: 388 KLYEIGAGTSEIRRMIIGR 406
           ++  I  GT+EI + +I R
Sbjct: 363 RVQRIYGGTNEIMKEVISR 381


Lambda     K      H
   0.319    0.135    0.396 

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: 382
Number of extensions: 21
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: 412
Length of database: 386
Length adjustment: 31
Effective length of query: 381
Effective length of database: 355
Effective search space:   135255
Effective search space used:   135255
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: 50 (23.9 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