GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Sphingomonas wittichii RW1

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate WP_012048726.1 SWIT_RS12735 aminotransferase

Query= SwissProt::P96847
         (388 letters)



>NCBI__GCF_000016765.1:WP_012048726.1
          Length = 374

 Score =  326 bits (835), Expect = 8e-94
 Identities = 176/377 (46%), Positives = 241/377 (63%), Gaps = 9/377 (2%)

Query: 11  VPPFYVMDVWLAAAERQRTHG-DLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVALG 69
           V PF  +++    A R  T G  ++++  GQPS G P  V   A AA+  +++GY  +  
Sbjct: 5   VQPFRAIEI-SGLARRLATEGRSVLHMEFGQPSMGPPRKVLDVARAAIDNDRMGYWES-- 61

Query: 70  IPELRDAIAADYQRRHGITVEPDAVVITTGSSGGFLLAFLACFDAGDRVAMASPGYPCYR 129
            P L++ +AA Y  R+G+ ++P   ++T G+S   +LA   CF AG R+AMA PGY  YR
Sbjct: 62  -PALKERLAALYADRYGVAIDPSRFLLTCGASPALVLALSICFPAGARIAMARPGYVAYR 120

Query: 130 NILSALGCEVVEIPCGPQTRFQPTAQMLAEIDPPLRGVVVASPANPTGTVIPPEELAAIA 189
           N + AL    VE+PCG ++RFQ TA+ LA I+P   GV++ASPANPTGT+I  +EL AIA
Sbjct: 121 NTVRALNMVPVELPCGAESRFQLTAEALAAIEPAPDGVIIASPANPTGTIIGGDELRAIA 180

Query: 190 SWCDASDVRLISDEVYHGLVYQGAPQTSCAWQTSRNAVVVNSFSKYYAMTGWRLGWLLVP 249
             C    +R++SDE+YH L Y G P  S A +   +AV+++SFSKYY M GWRLGWLLVP
Sbjct: 181 EVCRRRGIRILSDEIYHALSY-GEPCRSMA-EYDPDAVIISSFSKYYCMPGWRLGWLLVP 238

Query: 250 TVLRRAVDCLTGNFTICPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLRRIG 309
             L        G   + PP LSQ AA++A   +AT E D N+A YA NR+ LL+ L ++G
Sbjct: 239 PDLVERAWSYLGCLFLTPPTLSQHAALAAL--DATEELDANVAVYAGNRARLLEALPQMG 296

Query: 310 IDRLAPTDGAFYVYADVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRISFAG 369
           + R+AP DGAFY+YAD+   T DS+ FC KLL DTG+A  PGID D   G  F R+SFA 
Sbjct: 297 LRRIAPPDGAFYIYADIGHLTDDSMGFCRKLLLDTGLATGPGIDHDPVDGHRFFRLSFAI 356

Query: 370 PSGDIEEALRRIGSWLP 386
            + ++E+AL+R+  WLP
Sbjct: 357 SAEEVEKALQRLADWLP 373


Lambda     K      H
   0.321    0.136    0.416 

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: 479
Number of extensions: 26
Number of successful extensions: 4
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: 388
Length of database: 374
Length adjustment: 30
Effective length of query: 358
Effective length of database: 344
Effective search space:   123152
Effective search space used:   123152
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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