GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Herbaspirillum seropedicae SmR1

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate HSERO_RS15115 HSERO_RS15115 aminotransferase

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__HerbieS:HSERO_RS15115
          Length = 385

 Score =  172 bits (436), Expect = 1e-47
 Identities = 109/362 (30%), Positives = 190/362 (52%), Gaps = 13/362 (3%)

Query: 24  VAQHEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKAD 83
           +A  +  ++L  G PDF     + AA  +A+ E +  Y P AG   LR+A+   ++K   
Sbjct: 24  LASEKGAVNLGQGFPDFHCDPALVAAVTQAMQEGLNQYPPMAGVPVLREAIAEKVEKLYG 83

Query: 84  FNYDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIV--D 141
             YD  SEI +T GA+Q I  +    + PGDEVI+  P+Y  Y P I L G  PV V  +
Sbjct: 84  HRYDPVSEITVTAGATQGILTSVLCAVHPGDEVIVIEPVYDCYVPAIELAGGVPVFVQME 143

Query: 142 TTSHGFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSDE 201
             + G+ +    ++ A+TP T+ +++  P NPTG  +   ++ ++A +++G ++ +LSDE
Sbjct: 144 VGAQGYSIPWDKVKAAVTPKTRMIMVNTPHNPTGSVMRAADVAALADIVRGTDILILSDE 203

Query: 202 IYSELTYD-RPHYSIATY--LRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQ 258
           +Y  + YD +PH S+A +  L +++ + +   K++ +TGW++G++ AP  +     KVHQ
Sbjct: 204 VYEHMVYDGQPHESLARHPELAERSFINSSFGKTYHVTGWKVGYVAAPAALTAEFRKVHQ 263

Query: 259 YNVSCASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSMGLDVVKPSGAFYIF 318
           +NV   ++  Q   L A        L +   Y+ + D     L +   +++   G +  F
Sbjct: 264 FNVFTVNTPVQ-YGLAAYMKDPAPYLDLPAFYQHKRDLFRTGLANTRFELLPSQGTY--F 320

Query: 319 PSIKSFGMTSF---DFSMALLEDAGVALVPGSSF--STYGEGYVRLSFACSMDTLREGLD 373
             +K   +++    +F   L  + GVA +P S+F  +    G VR  FA   +TL+  L+
Sbjct: 321 QCVKYGAISALPEAEFCKWLTSEIGVAAIPVSAFYNTPRESGIVRFCFAKKDETLQLALE 380

Query: 374 RL 375
           RL
Sbjct: 381 RL 382


Lambda     K      H
   0.319    0.135    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: 321
Number of extensions: 21
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: 393
Length of database: 385
Length adjustment: 30
Effective length of query: 363
Effective length of database: 355
Effective search space:   128865
Effective search space used:   128865
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 Apr 09 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