GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaH in Clostridium acetobutylicum ATCC 824

Align Peroxisomal multifunctional enzyme A; MFE-A; MFE-1; EC 1.1.1.35 (characterized)
to candidate NP_350157.1 CA_C3574 3-ketoacyl-ACP reductase

Query= SwissProt::Q9NKW1
         (441 letters)



>NCBI__GCF_000008765.1:NP_350157.1
          Length = 249

 Score =  132 bits (332), Expect = 1e-35
 Identities = 89/249 (35%), Positives = 135/249 (54%), Gaps = 22/249 (8%)

Query: 8   KVVIVTGAGGGIGKVYALEFAKRGAKVVVNDLGGSHTGQGSSSKAADKVVEEIKAAGGTA 67
           KV +VTGAG G+G+  AL+ A  GA +VVN          SS     K+++EI+  G  A
Sbjct: 8   KVAVVTGAGRGLGRAIALKLAAEGANLVVN--------YRSSEAETQKLIKEIEELGSKA 59

Query: 68  VA---NYDSVEDGEKIVQTAMDSFGGVDILINNAGILRDVSFGKMTDGDWDLVYRVHAKG 124
           VA   +    ++ E I++ A+D +G VDIL+NNAGI +D    +M + D+D V  V+ KG
Sbjct: 60  VAVKADISKYDEAETIIKKALDEYGTVDILVNNAGITKDNLLLRMKEEDFDSVINVNLKG 119

Query: 125 AYKLSRAAWNHMREKNFGRIIMTSSAAGLYGNFGQANYGSMKMALVGLSNTLAQEGKSKN 184
           A+   +     M +K  G+II  SS  GL GN GQ NY + K  ++G++ ++A+E  S+ 
Sbjct: 120 AFNCIKHTSRVMLKKKSGKIINISSVIGLIGNAGQVNYAAAKAGIIGMTKSVAKELASRG 179

Query: 185 IHCNTIAP-IAASRLT--------ESVMPPEILEQM-KPDYIVPLVLYLCHQ-DTTETGG 233
           I  N +AP I  S +T        ES++    L ++ + + +  LVL+L     +  TG 
Sbjct: 180 ITVNAVAPGIIKSDMTDALTDKQRESIVAAVPLNKVGEAEDVANLVLFLASDLSSYITGQ 239

Query: 234 VFEVGAGWV 242
           V  V  G V
Sbjct: 240 VINVDGGMV 248



 Score = 25.8 bits (55), Expect = 0.002
 Identities = 20/71 (28%), Positives = 35/71 (49%), Gaps = 4/71 (5%)

Query: 371 ALDLKNGSGSIVVGAGSTKPNVTITVSDEDFVDIMTGKLNAQSAFTKGKLKISGNMGLAT 430
           ALD       +V  AG TK N+ + + +EDF  ++   +N + AF    +K +  + L  
Sbjct: 79  ALDEYGTVDILVNNAGITKDNLLLRMKEEDFDSVI--NVNLKGAF--NCIKHTSRVMLKK 134

Query: 431 KLGALMQGSKL 441
           K G ++  S +
Sbjct: 135 KSGKIINISSV 145


Lambda     K      H
   0.313    0.131    0.371 

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: 230
Number of extensions: 14
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 441
Length of database: 249
Length adjustment: 28
Effective length of query: 413
Effective length of database: 221
Effective search space:    91273
Effective search space used:    91273
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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