GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Prosthecochloris aestuarii DSM 271

Align Succinylornithine transaminase; SOAT; Succinylornithine aminotransferase; EC 2.6.1.81 (characterized)
to candidate WP_012504789.1 PAES_RS00970 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::Q8ZPV2
         (408 letters)



>NCBI__GCF_000020625.1:WP_012504789.1
          Length = 431

 Score =  138 bits (348), Expect = 3e-37
 Identities = 103/325 (31%), Positives = 147/325 (45%), Gaps = 30/325 (9%)

Query: 22  PFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPALREALNEQANRFWHIGNGYTN- 80
           P    +G+G+ + D  G  Y+D+ G      LG  HP +  AL     +   IG  +   
Sbjct: 36  PIYMAKGQGAYMTDVDGNTYLDYVGSWGPFILGSMHPRITAALEHTLTK---IGTSFGTP 92

Query: 81  -EPALRLAKKLIDATFA-ERVFFCNSGAEANEAALKLARKYAHDRVGNHKSGIVAFKNAF 138
            E  + +A+ L     + E V   NSG EA  +A++LAR Y        +  I+ F+  +
Sbjct: 93  IEMEIEIAELLCQIVPSIEMVRMVNSGTEATMSAVRLARGYTS------RDKIIKFEGCY 146

Query: 139 HGR-TLFTVSAG------GQPTYSQDFAPLPPDIRHAAYNDLNSASALIDDNT---CAVI 188
           HG    F + AG      G P           D  +A YND+ S   L+++N     A+I
Sbjct: 147 HGHGDSFLIKAGSGALTLGAPDSPGVTKGTANDTLNAKYNDIESVRLLVNENKGNIAAII 206

Query: 189 VEPVQGEGGVIPATKAFLQGLRELCDRHQALLIFDEVQTGVGRTGELYAYMHYGVTPDIL 248
           +EPV G  GVIPA   FLQ LR+LC     +LIFDEV  G  R     A   YGVTPD+ 
Sbjct: 207 IEPVAGNTGVIPAKPGFLQALRDLCTEEGIVLIFDEVMCGF-RVALGGAQERYGVTPDLT 265

Query: 249 TTAKALGGGFPIGAMLTTQDYASVMTP---GTHGTTYGGNPLATAVAGKVLDIINT---- 301
           T  K +GGG P+GA    ++    + P        T  GNPLA     + L I+      
Sbjct: 266 TMGKIIGGGLPVGAFGGKREIMERIAPLGDVYQAGTLSGNPLALTAGLETLKILRDENPY 325

Query: 302 PEMQNGVRQRHDAFIERLNTLNVRF 326
           PE++       + F   +N L + +
Sbjct: 326 PELERKAAFLEEGFRNNMNKLGLNY 350


Lambda     K      H
   0.320    0.137    0.413 

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: 427
Number of extensions: 30
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: 408
Length of database: 431
Length adjustment: 32
Effective length of query: 376
Effective length of database: 399
Effective search space:   150024
Effective search space used:   150024
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 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