GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Methylocapsa acidiphila B2

Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate WP_051335635.1 METAC_RS0116365 aspartate aminotransferase family protein

Query= curated2:Q81M98
         (386 letters)



>NCBI__GCF_000427445.1:WP_051335635.1
          Length = 476

 Score =  231 bits (590), Expect = 2e-65
 Identities = 139/339 (41%), Positives = 197/339 (58%), Gaps = 17/339 (5%)

Query: 1   MISHLFQTYGRRTVEFVKGNGTKVIDNNGKQYLDFTSGIGVCNLGHCHPTVMKAVQEQLN 60
           M+  + QT G   V F  G G  + D  G++YLD  SG GV  +G  HP + +A+   L 
Sbjct: 41  MMVRVLQTIGF-DVGFRCGRGQYLFDREGERYLDLLSGFGVFGIGRNHPALRQALGAVLE 99

Query: 61  DIWHISNLFTNSLQEEVASLLTENIA-----LDYVFFCNSGAEANEAALKLARKHTGKSL 115
               + NL    +   +A LL E +      LD VFF NSG EA EAALK AR  TG+  
Sbjct: 100 S--DLPNLVQMDVSV-LAGLLAERLLRYAPYLDKVFFTNSGTEAVEAALKFARSATGRPG 156

Query: 116 VVTCEQSFHGRTFGTMSATGQNKVKEGFGPLLPSFLHTPFNDIKALKEVMNE-EVAAVMV 174
           VV C+ +FHG T+G +S  G    ++GFGPL+P  +  PF+D+ AL   +++ +VAA +V
Sbjct: 157 VVHCDHAFHGLTYGALSLNGDEIFRDGFGPLIPGCVQIPFDDLAALDRALSKRDVAAFIV 216

Query: 175 EVVQGEGGVIPADLSFLKEIETLCKKFGSLFIIDEVQTGIGRTGTLFAYEQMGIDPHIVT 234
           E +QG+G  IP DL +L+  + LC+K+G+LFI DEVQTG+GRTG   A E  G++P +V 
Sbjct: 217 EPIQGKGVNIPNDL-YLRGAQALCRKYGTLFIADEVQTGLGRTGKFLAIEHWGVEPDMVL 275

Query: 235 TAKALGNG-IPVGAMIGRKEL-----GTSFTAGSHGSTFGGNYVAMAAAKEVLQVSKRLS 288
            AKAL  G  PVGA++ RK +          A  HGSTF  N +AMAA    L V +   
Sbjct: 276 LAKALSGGHAPVGAVLARKAIFEKVFNRMDRAVVHGSTFAKNDLAMAAGLATLDVIESEG 335

Query: 289 FLKEVQEKGEYVLQKLQEELQHVECIQNIRGKGLMVGIE 327
            ++  ++KG  +L   +   +  E ++ +RGKGLM+G+E
Sbjct: 336 LVRNAEQKGARLLAAFEAMAERHELVKTVRGKGLMIGVE 374


Lambda     K      H
   0.319    0.136    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: 345
Number of extensions: 13
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: 386
Length of database: 476
Length adjustment: 32
Effective length of query: 354
Effective length of database: 444
Effective search space:   157176
Effective search space used:   157176
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: 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