GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Pseudomonas fluorescens FW300-N2E2

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate Pf6N2E2_1496 Aspartate aminotransferase (EC 2.6.1.1)

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1496
          Length = 403

 Score =  188 bits (477), Expect = 3e-52
 Identities = 124/365 (33%), Positives = 196/365 (53%), Gaps = 23/365 (6%)

Query: 29  DVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKKKADFNYDA 88
           D++ LT G+PDF TP H+K AA  AI    T YTP  G   LR AVQ  +  +   +Y  
Sbjct: 33  DILDLTTGEPDFDTPTHIKQAAYAAIAAGATKYTPTPGVKALRVAVQRKLCTENQLDYPL 92

Query: 89  ESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIVDT-TSHGF 147
           ES I+I  GA Q I  AF   L  GDEV++P P +P +   +   G +PV ++     G 
Sbjct: 93  ES-IVIANGAKQIIFNAFAATLDDGDEVLVPTPYWPSFPDSVRFNGGEPVFIECGLEQGC 151

Query: 148 KLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGR-NVFVLSDEIYSEL 206
           KLT + +E  +   T+ ++L  P NP+G   SE EL+ +A +L+   +V +L DE+Y  +
Sbjct: 152 KLTPQQLEQHIGERTRWLILNSPGNPSGAVYSEAELQGLAQVLRRHAHVLILLDELYEHI 211

Query: 207 TYD----RPHYSIATYLRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVHQYNVS 262
            +D    +   ++A  L+ + +++ G+SK+++MTGWRIGF   P+ ++  +  V   + S
Sbjct: 212 RFDGRAAQNLLNVAPDLQARCLLVGGVSKTYAMTGWRIGFGAGPQALSDAMTVVQSQSTS 271

Query: 263 CASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSM-GLDVVKPSGAFYIFPSI 321
            ASS+ Q AAL A   G +        Y++R D +   L ++ GL+V++P G F++F  +
Sbjct: 272 GASSVGQAAALAAFEGGLEFLPEQVAAYRQRRDGLVSTLRTVEGLEVLEPHGGFFVF--V 329

Query: 322 KSFGM----------TSFDFS-MALLEDAGVALVPGSSFSTYGEGYVRLSFACSMDTLRE 370
           +  G+             D   +A L D GVA V GS++      + RLS A + +T+ E
Sbjct: 330 RCAGLLGRYRPDGQRLEHDADVVAYLLDEGVAGVAGSAYGL--SPWFRLSIATATETVAE 387

Query: 371 GLDRL 375
              R+
Sbjct: 388 AGRRI 392


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: 330
Number of extensions: 18
Number of successful extensions: 5
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: 403
Length adjustment: 31
Effective length of query: 362
Effective length of database: 372
Effective search space:   134664
Effective search space used:   134664
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