GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Thioalkalivibrio thiocyanodenitrificans ARhD 1

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (characterized)
to candidate WP_018231675.1 THITHI_RS0103415 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= SwissProt::P40732
         (405 letters)



>NCBI__GCF_000378965.1:WP_018231675.1
          Length = 460

 Score =  164 bits (414), Expect = 6e-45
 Identities = 112/349 (32%), Positives = 168/349 (48%), Gaps = 35/349 (10%)

Query: 32  KGSRVW--DQQGKEYIDFAGGIAVTALGHCHPALVEALKSQGETLWHTSNV-FTNEPALR 88
           +G  VW  D  G  YID      V   GH +P + +A++ Q + L H     FT+EP +R
Sbjct: 34  RGEGVWLEDFDGNRYIDAVSSWWVNLFGHANPRINQAIRDQLDRLEHVILAGFTHEPVIR 93

Query: 89  LGRKLIDAT--FAERVLFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRSL 146
           L  KL+  T     R  F +SG+ A E A K++ HY   R    KT+ I   N++HG +L
Sbjct: 94  LSEKLVAITPPGLSRCFFADSGSAAVEVALKMSYHYWRNRGQGGKTRFICLTNSYHGETL 153

Query: 147 FTVSVGGQPKYSDGFGPKPADIIHVPFNDLHAVKAVMD--------------------DH 186
             +SVG  P Y + +       I V   D +  +A  D                      
Sbjct: 154 GALSVGDVPLYKETYKSLLMQSITVQAPDCYLREAGEDCAQLAERMFVHMEQALARHAHE 213

Query: 187 TCAVVVEP-IQGEGGVQAATPEFLKGLRDLCDEHQALLVFDEVQCGMGRTGDLFAYMHYG 245
           TCAV+VEP +Q  GG++   P +L  LR+ CD H   L+ DE+  G GRTG +FA    G
Sbjct: 214 TCAVIVEPLVQCAGGMRMYDPRYLSLLREACDRHGMHLIADEIAVGFGRTGTMFACEQAG 273

Query: 246 VTPDILTSAKALGGGF-PVSAMLTTQEIASAFH-------VGSHGSTYGGNPLACAVAGA 297
           +TPD L  +K L GG+ P+SA++TT+ +  AF+          H  +Y GNPLACA A  
Sbjct: 274 ITPDFLCLSKGLTGGYLPLSAVVTTEGVYQAFYDEYEKLNAFLHSHSYTGNPLACAAALG 333

Query: 298 AFDIINTPEVLQGIHTKRQQFVQHLQAIDEQFDIFSDIRGMGLLIGAEL 346
              I    +V+       +   + L  + +  ++ +++R  G++   E+
Sbjct: 334 TLGIFEGEDVIGNNRHLAKVMAEALAPLQDHPNV-AEVRQTGMIAAVEM 381


Lambda     K      H
   0.322    0.137    0.412 

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: 428
Number of extensions: 26
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 405
Length of database: 460
Length adjustment: 32
Effective length of query: 373
Effective length of database: 428
Effective search space:   159644
Effective search space used:   159644
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 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