GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Pseudomonas fluorescens FW300-N1B4

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate Pf1N1B4_4425 Aspartate aminotransferase (EC 2.6.1.1)

Query= BRENDA::Q7NDX4
         (392 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4425
          Length = 403

 Score =  141 bits (356), Expect = 3e-38
 Identities = 111/373 (29%), Positives = 179/373 (47%), Gaps = 23/373 (6%)

Query: 29  GVDIINMGIGDPDKPTPPVVLEAMHAAIDDPSTHNYPPYKGTKAYREAAAAWFERRFGVG 88
           G DI+++ IG+PD  TP  + +A +AAI   +T  Y P  G KA R A      +   + 
Sbjct: 31  GRDILDLTIGEPDFDTPEHIKQAAYAAIAGGAT-KYTPTPGVKALRIAVQRKLRQENHLD 89

Query: 89  GFHPDTEVISSIGSKEAIHNTFLAFVDPGDYTLIPDPAYPVYRTSTIFAGGE--FFAMPL 146
             +P   ++ + G+K+ I N F A +D GD  L+P P +P +  S  F GGE  F    L
Sbjct: 90  --YPLESIVIANGAKQIIFNAFAATLDDGDQVLVPTPYWPSFPDSVRFNGGEPVFIECGL 147

Query: 147 LPENQLLPDLEAVPETVARKAKLLWLNYPNNPTGAVASLEFFEKVVHFAKKH-DILVCHD 205
               +L    E + + +  + + L LN P NP+GAV S    + +    ++H  +L+  D
Sbjct: 148 AQGCKLTA--EQLEQYIGERTRWLILNGPGNPSGAVYSAAELQALAEVLRRHPQVLILLD 205

Query: 206 NAYSEMAYDGYKPPSILQV-PGARDVAIEFLSCSKAYNMTGWRVGFVIGNRTGIAGLGQV 264
             Y  + +DG    S+L V P  +   +     SK Y MTGWR+GF  G +     +  V
Sbjct: 206 ELYEHIRFDGRPAQSLLSVAPDLQSRCLLVGGVSKTYAMTGWRIGFGAGPQALANAMTVV 265

Query: 265 KTNIDSGVFKAIQQAAIAAFGLDDERLHALMAVYQNRRNIIVEGLRSL-GWPLEAPKATL 323
           ++   SG     Q AA+AAF    + L + +A YQ RR+++V  LR + G  +  P+   
Sbjct: 266 QSQSTSGASSVGQAAALAAFDGGLDFLRSQVAAYQQRRDLLVSALRKVDGLEVLEPQGGF 325

Query: 324 YV----------WAPIPKSFGSSVEFVGALLDKCGIIVPPGNGYGEHGEGFFRIALTVPD 373
           +V          + P  +   +  + V  LL++ G+    G+ YG     +FR+++    
Sbjct: 326 FVFIRCAGLLGRYRPDGQRLQTDADVVAYLLEE-GVAGVAGSAYGL--SPWFRLSIATAT 382

Query: 374 ERMREAIGRMEAA 386
           E + EA  R+  A
Sbjct: 383 ETVAEAGRRIAQA 395


Lambda     K      H
   0.321    0.140    0.429 

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: 319
Number of extensions: 10
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: 392
Length of database: 403
Length adjustment: 31
Effective length of query: 361
Effective length of database: 372
Effective search space:   134292
Effective search space used:   134292
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