GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Saccharomonospora cyanea NA-134

Align [amino group carrier protein]-gamma-(L-lysyl)-L-glutamate aminotransferase (EC 2.6.1.118) (characterized)
to candidate WP_005457886.1 SACCYDRAFT_RS16640 acetylornithine transaminase

Query= BRENDA::Q93R93
         (395 letters)



>NCBI__GCF_000244975.1:WP_005457886.1
          Length = 395

 Score =  284 bits (727), Expect = 3e-81
 Identities = 159/362 (43%), Positives = 210/362 (58%), Gaps = 1/362 (0%)

Query: 31  IVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQAETLMAMPQTLPTPMRG 90
           +VRG+GA VWDA+G  Y+D V G  V  LGH +P VV AV RQ  T+             
Sbjct: 25  LVRGEGAVVWDADGRRYLDFVTGIAVNALGHAHPAVVSAVTRQIATIGHTSNLYLNEPAL 84

Query: 91  EFYRTLTAILPPELNRVFPVNSGTEANEAALKFARAHTGRKKFVAAMRGFSGRTMGSLSV 150
                L  +      +V   NSG EA EAA K AR  TGR   VA   GF GRTMG+L++
Sbjct: 85  TLAERLLELSGAGDGKVLFCNSGAEAVEAAFKLAR-RTGRSTVVATEGGFHGRTMGALAL 143

Query: 151 TWEPKYREPFLPLVEPVEFIPYNDVEALKRAVDEETAAVILEPVQGEGGVRPATPEFLRA 210
           T +P  R PF PLV  V  +P+ DV AL+RA+D +TAA ++EPVQGE GV     ++LRA
Sbjct: 144 TGQPAKRAPFEPLVPGVRHVPFGDVPALERAIDSDTAAFVVEPVQGENGVVVPGDDYLRA 203

Query: 211 AREITQEKGALLILDEIQTGMGRTGKRFAFEHFGIVPDILTLAKALGGGVPLGVAVMREE 270
           AREIT+  G LL++DE+QTG+GR G  FA++  GI PD++TLAK LGGG+PLG  +   E
Sbjct: 204 AREITRRHGVLLVVDEVQTGVGRLGSWFAYQQTGIQPDVVTLAKGLGGGLPLGACLAFGE 263

Query: 271 VARSMPKGGHGTTFGGNPLAMAAGVAAIRYLERTRLWERAAELGPWFMEKLRAIPSPKIR 330
            A     G HGTTFGGNP+  AAG+A +  +    L E  A LG      L  +  P +R
Sbjct: 264 AATLFEPGQHGTTFGGNPVCCAAGLAVLDTIAANGLLEHTAALGKEISAGLERLDHPLVR 323

Query: 331 EVRGMGLMVGLELKEKAAPYIARLEKEHRVLALQAGPTVIRFLPPLVIEKEDLERVVEAV 390
            VRG GL++G+ L    +  +A   +    L     P V+R  PPLV+ +E  + ++ A+
Sbjct: 324 TVRGAGLLLGVVLNSAVSAGVAAAAQRAGFLVNPVQPDVVRLAPPLVVSQEQADALLAAL 383

Query: 391 RA 392
            A
Sbjct: 384 PA 385


Lambda     K      H
   0.319    0.137    0.403 

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: 410
Number of extensions: 15
Number of successful extensions: 3
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: 395
Length of database: 395
Length adjustment: 31
Effective length of query: 364
Effective length of database: 364
Effective search space:   132496
Effective search space used:   132496
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 (21.7 bits)
S2: 50 (23.9 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