GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Dyella japonica UNC79MFTsu3.2

Align Probable aspartate aminotransferase; AspAT; EC 2.6.1.1; Transaminase A (uncharacterized)
to candidate N515DRAFT_2186 N515DRAFT_2186 alanine-synthesizing transaminase

Query= curated2:P63499
         (429 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2186
          Length = 410

 Score =  320 bits (819), Expect = 7e-92
 Identities = 173/394 (43%), Positives = 239/394 (60%), Gaps = 1/394 (0%)

Query: 31  SAKLQDVLYEIRGPVHQHAARLEAEGHRILKLNIGNPAPFGFEAPDVIMRDIIQALPYAQ 90
           SA L +V YEIRG + + +  LEA G  I+KLNIGNP  +GFE P  +   I   L  ++
Sbjct: 5   SAHLAEVRYEIRGALTRRSRELEAAGLPIIKLNIGNPGRYGFETPPHLRDAIAAHLRDSE 64

Query: 91  GYSDSQGILSARRAVVTRYELVPGFPRFDVDDVYLGNGVSELITMTLQALLDNGDQVLIP 150
            Y   QG+  AR  +  + +   G    +V+ +++GNGVSELI ++L+ALL  GD+VL+P
Sbjct: 65  AYGHEQGLEEARETIAAQ-QRARGARGVEVERIFVGNGVSELIDLSLRALLQPGDEVLLP 123

Query: 151 SPDYPLWTASTSLAGGTPVHYLCDETQGWQPDIADLESKITERTKALVVINPNNPTGAVY 210
           SPDYPLW+A+T L  G P +Y C    G  PD  ++E+ +T RT+A+V+INPNNPTGAVY
Sbjct: 124 SPDYPLWSAATILNDGQPRYYRCLAENGHLPDPDEIEALVTARTRAIVLINPNNPTGAVY 183

Query: 211 SCEILTQMVDLARKHQLLLLADEIYDKILYDDAKHISLASIAPDMLCLTFNGLSKAYRVA 270
             E+L ++V +A +H LLLL DEIYD+ILYD A+ + LA++A D+ C++F GLSK +R  
Sbjct: 184 PRELLERIVRIAERHHLLLLTDEIYDEILYDGAQFVPLATVAGDVPCVSFGGLSKVHRAC 243

Query: 271 GYRAGWLAITGPKEHASSFIEGIGLLANMRLCPNVPAQHAIQVALGGHQSIEDLVLPGGR 330
           GYR GW++++G       + + + LLA +RLC NV AQ A++ AL    +I  L  PGGR
Sbjct: 244 GYRVGWMSLSGDPVRTHDYRDALQLLAALRLCANVTAQWAVRPALESKPTIGALTSPGGR 303

Query: 331 LLEQRDIAWTKLNEIPGVSCVKPAGALYAFPRLDPEVYDIDDDEQLVLDLLLSEKILVTQ 390
           L E R +    +     +    P GALYAFPR+  +     DD    L LL  E +LV  
Sbjct: 304 LHEARRMILEGVANSEFLDLATPGGALYAFPRVRADRVPRFDDNAFALRLLEEESVLVVP 363

Query: 391 GTGFNWPAPDHLRLVTLPWSRDLAAAIERLGNFL 424
           G+ FN P   HLRL  LP    L     R+   L
Sbjct: 364 GSSFNVPDSRHLRLTLLPPPEQLREVFVRIERVL 397


Lambda     K      H
   0.320    0.138    0.419 

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: 527
Number of extensions: 29
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: 429
Length of database: 410
Length adjustment: 32
Effective length of query: 397
Effective length of database: 378
Effective search space:   150066
Effective search space used:   150066
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