GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Dyella japonica UNC79MFTsu3.2

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate N515DRAFT_0941 N515DRAFT_0941 isovaleryl-CoA dehydrogenase

Query= reanno::pseudo6_N2E2:Pf6N2E2_1146
         (375 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0941
          Length = 385

 Score =  255 bits (651), Expect = 2e-72
 Identities = 135/373 (36%), Positives = 218/373 (58%), Gaps = 2/373 (0%)

Query: 5   EEQTQIRDMARQFAEERLKPFAAEWDREHRFPREAIDEMAELGFFGMLVPEQWGGCDTGY 64
           EE   +R+    FAE+ + P A + D ++ FP +   +  E+G  GM +PE +GG   GY
Sbjct: 8   EELDLLRESVHAFAEKEIAPRATQIDHDNVFPADLWRKFGEMGLLGMTIPEAYGGTGLGY 67

Query: 65  LAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKFGNDEQKAKFLTPLASGAMLGAFALT 124
           LA+ + +EEI+   G+       H+++    +   GN+EQ+ K++  L SG  +GA A++
Sbjct: 68  LAHMVAMEEISRASGSVGLSYGAHSNLCVQNLFHNGNEEQRRKYIPRLCSGEYVGALAMS 127

Query: 125 EPQAGSDA-SSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPS-AGKRGISAF 182
           EP AGSD   S+  +A L GD +V NG K +IT+G +A V++V+  T P  AG R ++AF
Sbjct: 128 EPGAGSDVVGSMSCKAELRGDVWVANGTKMWITNGPDADVLLVYMRTAPRPAGSRCMTAF 187

Query: 183 IVPTDSPGYSVARVEDKLGQHASDTCQILFEDLKVPVGNRLGEEGEGYKIALANLEGGRV 242
           I+     G+S A+  DKLG   S+TC+++FED ++P  N +GE  EG ++ ++ L+  R+
Sbjct: 188 IIEKGMKGFSTAQKLDKLGMRGSNTCELVFEDCEIPAANIVGEVNEGVRVLMSGLDTERL 247

Query: 243 GIAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAA 302
            ++   +G+ +AA +    Y RER  F  PI     +  ++ADM T +  +R   +  A 
Sbjct: 248 VLSGGPLGLMQAAMDLVLPYVRERKQFNAPIGTFGMMQAKVADMYTALQSSRGFAYMVAR 307

Query: 303 LRDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYEG 362
             D G  + ++ +   L AS+ A KV   A+Q LGG GY+N+FP  R+ RD ++ +I  G
Sbjct: 308 EFDQGSKSRIDPAACLLNASQNAVKVALEAIQALGGNGYINEFPAGRLLRDAKLYEIGAG 367

Query: 363 TSDIQRMVISRNL 375
           T++I+RM+I R L
Sbjct: 368 TNEIRRMLIGREL 380


Lambda     K      H
   0.320    0.134    0.388 

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: 317
Number of extensions: 17
Number of successful extensions: 3
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: 375
Length of database: 385
Length adjustment: 30
Effective length of query: 345
Effective length of database: 355
Effective search space:   122475
Effective search space used:   122475
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.

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