GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Hydrogenovibrio kuenenii DSM 12350

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (uncharacterized)
to candidate WP_024850313.1 N745_RS0101155 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= curated2:P59317
         (406 letters)



>NCBI__GCF_000526715.1:WP_024850313.1
          Length = 442

 Score =  161 bits (407), Expect = 4e-44
 Identities = 112/345 (32%), Positives = 182/345 (52%), Gaps = 30/345 (8%)

Query: 32  QGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNALKTQGETLWHIS-NVFTNEPALRLG 90
           QGS I    G E VD          G+ HP +  A+  Q + + HI     T+EPA+ L 
Sbjct: 43  QGSVITLADGTELVDGMSSWWAALHGYNHPKIQQAMHEQIDIMPHIMFGGLTHEPAIELS 102

Query: 91  RKLIEAT--FAERVVFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRSLFT 148
           ++L++ T    ++V  ++SG+ A E A K+A  Y   +  P K +++   N +HG +  T
Sbjct: 103 KRLVKLTPEGLDKVFLVDSGSVAMEVAIKMALQYWVSKDQPNKNRLLTVRNGYHGDTFAT 162

Query: 149 VSV-----GGQPKYSD-----GFGPKPADIIHVPFN--DLHAVKAVMDDH---TCAVVVE 193
           ++V     G    +S+      F P+P     +  +  D++++K ++++H     AV +E
Sbjct: 163 MAVCDPVNGMHSLFSEILTQHYFAPEPEMGFDIESDNQDINSLKTMLEEHHNNIAAVTIE 222

Query: 194 PI-QGEGGVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVTPDILT 252
           PI QG GG+    P++L+ LR+LCD++  LL+ DE+  G GRTG LFA    G+TPDI+T
Sbjct: 223 PIVQGAGGMRFYRPDYLKQLRQLCDEYGVLLIADEIATGFGRTGKLFACEWAGITPDIMT 282

Query: 253 SAKAL-GGGFPVSAMLTTAEIASA-------FHPG--SHGSTYGGNPLACAVAGAAFDII 302
             K L GG   ++A L T +++          +PG   HG T+ GNPLACA A A  D++
Sbjct: 283 LGKTLTGGHISLAATLATTDVSDTISSNVGDLNPGLLMHGPTFMGNPLACAAAIANIDVL 342

Query: 303 NTPEVLEGIQAKRQHFVDHLQKIDQQYDVFSDIRGMGLLIGAELK 347
                 + IQ   +HF + L  + ++ +  +D R +G +   EL+
Sbjct: 343 MNSPWQDNIQRIEEHFTETLLPL-KELEGVADARVLGAIGVIELE 386


Lambda     K      H
   0.322    0.138    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: 474
Number of extensions: 26
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: 406
Length of database: 442
Length adjustment: 32
Effective length of query: 374
Effective length of database: 410
Effective search space:   153340
Effective search space used:   153340
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: 51 (24.3 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