GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Desulfovibrio vulgaris Hildenborough

Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate 207896 DVU2405 alcohol dehydrogenase, iron-containing

Query= BRENDA::P0DJA2
         (383 letters)



>MicrobesOnline__882:207896
          Length = 393

 Score =  388 bits (997), Expect = e-112
 Identities = 200/383 (52%), Positives = 262/383 (68%), Gaps = 6/383 (1%)

Query: 6   FYIPFVNEMGEGSLEKAIKDLNGSGFKNALIVSDAFMNKSGVVKQVADLLKAQGINSAVY 65
           F+IP V  +G G+ +   + +   G    LIV+D  + K+G++KQ+ DLL A  +  +VY
Sbjct: 10  FFIPRVTLIGIGASKAIPEKIKALGGSKPLIVTDMGIVKAGILKQITDLLDAAKMAYSVY 69

Query: 66  DGVMPNPTVTAVLEGLKILKDNNSDFVISLGGGSPHDCAKAIALVATNGGEVKDYEGIDK 125
           D  +PNPT   V +G+ + K N  D +I+LGGGS HDC K I LV  NGG++ D+EG+DK
Sbjct: 70  DETIPNPTDDNVHKGVDVYKKNKCDSLITLGGGSSHDCGKGIGLVVANGGKIHDFEGVDK 129

Query: 126 SKKPALPLMSINTTAGTASEMTRFCIITDEVRHVKMAIVDRHVTPMVSVNDPLLMVGMPK 185
           S +   P +++NTTAGTASEMTRFCIITD  R VKMAIVD  VTP ++++DPLLM+GMP 
Sbjct: 130 STQRMPPYLAVNTTAGTASEMTRFCIITDTSRKVKMAIVDWRVTPNIALDDPLLMLGMPP 189

Query: 186 GLTAATGMDALTHAFEAYSSTAATPITDACALKAASMIAKNLKTACDNGKDMPAREAMAY 245
            LTAATGMDALTHA EAY ST ATP+TDACA +A ++IA  L+ A  NG+D+ ARE M +
Sbjct: 190 ALTAATGMDALTHAVEAYVSTIATPMTDACAEQAITLIATFLRRAVANGQDLEARERMCF 249

Query: 246 AQFLAGMAFNNASLGYVHAMAHQLGGYYNLPHGVCNAVLLPHVLAYNASVVAGRLKDVGV 305
           AQ+LAGMAFNNASLG+VHAMAHQLGG+Y+LPHG CNA+LLPHV  +N      R   +  
Sbjct: 250 AQYLAGMAFNNASLGHVHAMAHQLGGFYDLPHGECNAILLPHVSKFNLIAKLDRYARIAQ 309

Query: 306 AMGLDIANLGDKEGAEATIQAVRDLAASIGIPANLTELG------AKKEDVPLLADHALK 359
            MG +IA L  +E AE  I A++ L+  +GIPA L  LG       K  D+ ++  +A K
Sbjct: 310 LMGENIAGLSTREAAERAISAIKCLSTDVGIPAGLVALGKRYGKDVKAADIAIMTKNAQK 369

Query: 360 DACALTNPRQGDQKEVEELFLSA 382
           DAC LTNPR     +V  ++ +A
Sbjct: 370 DACGLTNPRCPTDADVAAIYEAA 392


Lambda     K      H
   0.316    0.132    0.373 

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: 437
Number of extensions: 19
Number of successful extensions: 2
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: 383
Length of database: 393
Length adjustment: 30
Effective length of query: 353
Effective length of database: 363
Effective search space:   128139
Effective search space used:   128139
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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