GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Nocardioides dokdonensis FR1436

Align succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_068111454.1 I601_RS15155 acetylornithine transaminase

Query= BRENDA::O30508
         (406 letters)



>NCBI__GCF_001653335.1:WP_068111454.1
          Length = 396

 Score =  302 bits (773), Expect = 1e-86
 Identities = 171/379 (45%), Positives = 231/379 (60%), Gaps = 17/379 (4%)

Query: 17  MVPNYAPAAFIPVRGEGSRVWDQSGRELIDFAGGIAVTSLGHAHPALVKALTEQAQRIWH 76
           ++  + P     VRGEG+ VWD  G+E +D  GGIAV +LGHAHPALV A+T+Q   + H
Sbjct: 21  LMNTFGPPKLTLVRGEGAHVWDADGKEYVDLLGGIAVNALGHAHPALVAAVTDQLSTLGH 80

Query: 77  VSNVFTNEPALRLARKLVDATFAE--RVFLANSGAEANEAAFKLARRYANDVYGPQKYEI 134
           +SN FT+ P + LA KLV    A   +VFLANSGAEANEAAFK+ RR         +  +
Sbjct: 81  ISNFFTSVPQVELAEKLVALVGAGPGKVFLANSGAEANEAAFKMTRRTG-------RTHV 133

Query: 135 IAASNSFHGRTLFTVNVGGQPKYSDGFGPKFEGITHVPYNDLEALKAAISDKTCAVVLEP 194
           + A   FHGRT+  + +  +  Y + F P    +T VPY D++AL+ A+++ T A++LEP
Sbjct: 134 VVAEGGFHGRTMGALALTSKAAYREPFEPLPGDVTFVPYGDVDALREAVTETTAAILLEP 193

Query: 195 IQGEGGVLPAQQAYLEGARKLCDEHNALLVFDEVQSGMGRVGELFAYMHYGVVPDILSSA 254
           IQGE GV+ A   YL  AR L DE  ALL  DEVQ+GMGR G+ FA+  + VVPDIL+ A
Sbjct: 194 IQGEAGVVMAPAGYLRAARALADESGALLWLDEVQTGMGRTGDWFAHAGH-VVPDILTLA 252

Query: 255 KSLGGGFPIGAMLTTGEIAKHLSVGTHGTTYGGNPLASAVAEAALDVINTPEVLDGVKAK 314
           K LGGG+PIGA++  G  A  L  G HGTT+GG+P+A A A A +  I    +L+ V+  
Sbjct: 253 KGLGGGYPIGAVVGLGRAADLLEPGNHGTTFGGSPVACAAALAVIRTIEEDGLLEHVRRA 312

Query: 315 HERFKSRLQKIGQEYGIFDEIRGMGLLIGAALTDEWKGKARDVLNAAEKEAVMVLQASPD 374
            ER +  L    +      E+RG GLLIG  L  E    A  V+ AA++   +V   +P 
Sbjct: 313 GERLREGLAADAR----VTEVRGEGLLIGLDLVSE---TAAAVVEAAQRAGFIVNMPTPS 365

Query: 375 VVRFAPSLVIDDAEIDEGL 393
            +R AP LV+ DA+I+  L
Sbjct: 366 RIRLAPPLVLTDADIESFL 384


Lambda     K      H
   0.318    0.135    0.394 

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: 449
Number of extensions: 20
Number of successful extensions: 6
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: 396
Length adjustment: 31
Effective length of query: 375
Effective length of database: 365
Effective search space:   136875
Effective search space used:   136875
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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