GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Acidimicrobium ferrooxidans DSM 10331

Align succinyldiaminopimelate transaminase (EC 2.6.1.17); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_015798108.1 AFER_RS03385 class I and II aminotransferase

Query= BRENDA::Q82IK5
         (364 letters)



>NCBI__GCF_000023265.1:WP_015798108.1
          Length = 361

 Score =  174 bits (441), Expect = 3e-48
 Identities = 130/361 (36%), Positives = 171/361 (47%), Gaps = 34/361 (9%)

Query: 21  ARAAAHPDGIVDLSVGTPVDPVPELIQKALVAAADSPGYPTVWGTPELRDALTGWVERRL 80
           A AA     +VD S+G+PVDP P  +   L    +   YP   GTP L ++ T W     
Sbjct: 12  ALAADRHPFVVDASIGSPVDPPPAFVPHLLACQGEERAYPPAAGTPALVESATRWFH--- 68

Query: 81  GARGVT--HHHVLPIVGSKELVAWLPTQLGLGPGDK--VAHPRLAYPTYEVGARLARADH 136
             RGVT     V P +GSKE +  L   L     D+  V  P  AYPTY  GAR A  + 
Sbjct: 69  ALRGVTLPDGAVAPTMGSKEAIGTLAWLLRERRPDRGVVLIPGRAYPTYAEGARAAGCEI 128

Query: 137 VVYDDPTELDPT----------GLKLLWLNSPSNPTGKVLSKAELTRIVAWAREHGILVF 186
           V   D     P              + W+NSPSNPTG V        +VA AREHG ++ 
Sbjct: 129 VRVPDDCSGAPAFDAVAASVWDRTLVAWVNSPSNPTGAVYDPGP---VVALAREHGAVLA 185

Query: 187 SDECYLELGWEADPVSVLHPDVCGGSYEGIVSVHSLSKRSNLAGYRAAFLAGDPAVLGPL 246
           SDE Y +  W  +  S L   +     EG +++ SLSKRSNLAG R   +AGDP ++  +
Sbjct: 186 SDEAYGDFVWSGEAPSALRAGL-----EGTLALVSLSKRSNLAGLRLGLVAGDPMLVDEV 240

Query: 247 LQIRKHGGMMTSAPTQAAVVAALGDDAHVREQRERYAARRTALR---DALLSHGFRIEHS 303
           +  R+  G++ S P+QA    AL D+ HV EQR RYA R   L    +A+     R+   
Sbjct: 241 VARRRALGLLASGPSQAVAAEALADEGHVAEQRSRYAGRLRRLARVIEAVADVPVRV--P 298

Query: 304 EASLYLWATRGESCWDTVAH--LADLGILVAPGDFYGSAGEQFVRVALTATDERVAAAVR 361
           +  +YLW    +      A      LGI+VA G  YG     FVR+A T  D  + A   
Sbjct: 299 DGGIYLWVRAPDDDGAAFARWLATRLGIVVADGADYGD--RAFVRIAATVKDRAIDALWE 356

Query: 362 R 362
           R
Sbjct: 357 R 357


Lambda     K      H
   0.319    0.135    0.420 

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: 463
Number of extensions: 32
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: 364
Length of database: 361
Length adjustment: 29
Effective length of query: 335
Effective length of database: 332
Effective search space:   111220
Effective search space used:   111220
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: 49 (23.5 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