GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD'B in Chlorobaculum parvum NCIB 8327

Align Succinylornithine transaminase; SOAT; Succinylornithine aminotransferase; EC 2.6.1.81 (characterized)
to candidate WP_012501411.1 CPAR_RS00790 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::Q8ZPV2
         (408 letters)



>NCBI__GCF_000020505.1:WP_012501411.1
          Length = 431

 Score =  140 bits (353), Expect = 7e-38
 Identities = 109/327 (33%), Positives = 151/327 (46%), Gaps = 34/327 (10%)

Query: 22  PFIPVRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPALREALNEQANRFWHIGNGYTNE 81
           P    +G+G+ + D  G  Y+D+ G      LG  HP L  A+ E   R      G   E
Sbjct: 36  PIYMAKGQGAYMTDVDGNTYLDYVGSWGPFILGSMHPRLTAAI-EYTLRNIGTSFGTPIE 94

Query: 82  PALRLAKKLIDATFA-ERVFFCNSGAEANEAALKLARKYAHDRVGNHKSGIVAFKNAFHG 140
             + +A+ L     + E V   NSG EA  +A++LAR Y        K  I+ F+  +HG
Sbjct: 95  IEIEIAELLCQIVPSLEMVRMVNSGTEATMSAVRLARGYTG------KDKIIKFEGCYHG 148

Query: 141 R-TLFTVSAG------GQPTYSQDFAPLPPDIRHAAYNDLNSASALIDDN---TCAVIVE 190
               F + AG      G P           D  +A YND+ S  A++++N     A+I+E
Sbjct: 149 HGDSFLIKAGSGVLTLGDPDSPGVTKGTANDTLNATYNDIESVKAIVNENKGQVAAIIIE 208

Query: 191 PVQGEGGVIPATKAFLQGLRELCDRHQALLIFDEVQTG----VGRTGELYAYMHYGVTPD 246
           PV G  GVIPA K FL  LRELCD    +LIFDEV  G    +G   EL     YGVTPD
Sbjct: 209 PVAGNTGVIPAKKEFLVALRELCDAEGIVLIFDEVMCGFRVALGGAQEL-----YGVTPD 263

Query: 247 ILTTAKALGGGFPIGAMLTTQDYASVMTP-GT--HGTTYGGNPLATAVAGKVLDIINT-- 301
           + T  K +GGG P+GA    +     + P G+     T  GNPLA     + L I+    
Sbjct: 264 LTTMGKIIGGGLPVGAFGGKRKIMENIAPLGSVYQAGTLSGNPLALTAGLETLKILMEEN 323

Query: 302 --PEMQNGVRQRHDAFIERLNTLNVRF 326
             PE++         F + +N L + +
Sbjct: 324 PYPELERKAAFLEAGFKDNMNKLGLNY 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: 461
Number of extensions: 34
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: 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