GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Sulfurimonas denitrificans DSM 1251

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (characterized)
to candidate WP_011372739.1 SUDEN_RS05820 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::P18335
         (406 letters)



>NCBI__GCF_000012965.1:WP_011372739.1
          Length = 430

 Score =  121 bits (304), Expect = 3e-32
 Identities = 100/328 (30%), Positives = 150/328 (45%), Gaps = 25/328 (7%)

Query: 31  GQGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNALKTQGETLWHISNVFTNEPALRLG 90
           G G+ + D  G  YVDF         GH   ++ +A+    E + H  +      A    
Sbjct: 41  GSGAYLTDIDGNRYVDFVQSWGPLLFGHRDESIESAVI---EAVKHGLSFGAPTQAESDL 97

Query: 91  RKLIEATF--AERVVFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRS--L 146
             L+ + F   E++ F++SGTEA  +A +LAR Y           I+ F   +HG S  L
Sbjct: 98  AALVISMFDSIEKIRFVSSGTEAVMSAIRLARGYTNC------DDIVKFTGCYHGHSDSL 151

Query: 147 FTVSVGGQPKYSDGFGPK-PADI----IHVPFNDLHAVKAVMDDH--TCAVVVEPIQGEG 199
              +  G   + +   P  PAD     +   +N++ +VK    D      V++EPI G  
Sbjct: 152 LVQAGSGAATFGNPSSPGVPADFTKHTLLAEYNNIESVKKCFSDSKDVACVIIEPIAGNM 211

Query: 200 GVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVTPDILTSAKALGG 259
           G+  A  EFL+ LRELCD + ALL+FDEV  G  R     A    GV PDI+T  K +GG
Sbjct: 212 GLVPADKEFLRELRELCDANGALLIFDEVMSGF-RASVHGAESITGVKPDIVTLGKVIGG 270

Query: 260 GFPISAMLTTAEIASAFHPGS---HGSTYGGNPLACAVAGAAF-DIINTPEVLEGIQAKR 315
           G P+ A    AEI +   P        T  GNP+A A   AA   +    +++  + ++ 
Sbjct: 271 GMPVGAFGARAEIMAKLSPEGPVYQAGTLSGNPVAMAAGLAAITKLKQNGQIISVLNSRA 330

Query: 316 QRFVDHLQKIDQQYDVFSDIRGMGLLIG 343
            R V+ +Q+  + Y +   I   G + G
Sbjct: 331 TRLVEGMQEAAKTYGIAMQIDTRGSMFG 358


Lambda     K      H
   0.322    0.138    0.415 

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: 408
Number of extensions: 26
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: 406
Length of database: 430
Length adjustment: 32
Effective length of query: 374
Effective length of database: 398
Effective search space:   148852
Effective search space used:   148852
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 (21.9 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