GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Desulfotalea psychrophila LSv54

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (characterized)
to candidate WP_011188057.1 DP_RS04140 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::P18335
         (406 letters)



>NCBI__GCF_000025945.1:WP_011188057.1
          Length = 430

 Score =  135 bits (341), Expect = 2e-36
 Identities = 93/313 (29%), Positives = 148/313 (47%), Gaps = 29/313 (9%)

Query: 30  KGQGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNALKTQGETLWHISNVFTNEPALRL 89
           + +GS I+D  G++Y+DF        +GH HP ++ A+  Q   ++  S        + L
Sbjct: 40  RAEGSYIYDADGQKYLDFVNSWGPMIMGHAHPDIIKAI--QDAAVYGTSYGAPTSSEVDL 97

Query: 90  GRKLIEATFA-ERVVFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRS--- 145
              ++EA  + E+V F++SGTEA  +A +LAR Y        K  I+ F   +HG +   
Sbjct: 98  ASMVVEAVPSIEKVRFVSSGTEATMSAVRLARGYTG------KNVIVKFDGCYHGHADSF 151

Query: 146 -------LFTVSVGGQPKYSDGFGPKPADIIHVPFNDLHAVKAVMDD---HTCAVVVEPI 195
                  + T+ + G P   +       + I +P+N + A++  + D   +   V+VEP+
Sbjct: 152 LVKAGSGVLTLGIPGSPGVPEDI---VKNTISIPYNSVEALETTLRDADLNIACVIVEPV 208

Query: 196 QGEGGVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVTPDILTSAK 255
            G  G     P FLQ LRE+  +   +L+FDEV  G  R     A  +YGVTPD+    K
Sbjct: 209 AGNMGCVPPAPGFLQKLREITAEEGIVLIFDEVITGF-RLSYGGAQQYYGVTPDLTCLGK 267

Query: 256 ALGGGFPISAMLTTAEIASAFHPGS---HGSTYGGNPLACAVAGAAFDIINTPEVLEGIQ 312
            +GGG P+ A    A+I ++  P        T  GNPLA A   AA  ++      E + 
Sbjct: 268 IIGGGLPVGAYGGKADIMNSVAPDGPVYQAGTLSGNPLAMAAGKAALKLLQQDGFYEDLN 327

Query: 313 AKRQRFVDHLQKI 325
            K   + D L ++
Sbjct: 328 QKSAAYADGLLEV 340


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: 423
Number of extensions: 21
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: 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 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