GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Methanobacterium lacus AL-21

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (uncharacterized)
to candidate WP_013644768.1 METBO_RS05880 homoserine dehydrogenase

Query= curated2:Q58997
         (336 letters)



>NCBI__GCF_000191585.1:WP_013644768.1
          Length = 339

 Score =  361 bits (926), Expect = e-104
 Identities = 191/335 (57%), Positives = 243/335 (72%), Gaps = 2/335 (0%)

Query: 1   MDIIIVGFGAIGKGIAKVLYDKKDYLKKNYE-EFKVVAITDSSGAAIDEDGLDLLKAIEV 59
           M + I+GFGA+G G+ KVL  K D L   Y  +  VVA+TD SGAA++ +GLDL   IE 
Sbjct: 1   MKLCILGFGAVGMGVVKVLSMKNDMLIDKYGLDISVVAVTDRSGAAVNPEGLDLQLLIET 60

Query: 60  KEKTGKIKNYPEKGRE-MSSIDVIKEVDADVVVEVTPSNLETGDPAKTHILESFKNKKHV 118
           KE T KI +YPE G   + S +V++ V+ D +VEVTP+N++ G+PA TH++E+ K  + V
Sbjct: 61  KENTNKISDYPEYGVPGLDSAEVVETVEFDCLVEVTPTNIDHGEPANTHMMETLKKGRDV 120

Query: 119 VTANKGPLALCYKELIEEAKKHGVIFRHEASVGGAMPIINLAKETLAGNEILSIRGILNG 178
           VT+NKGPL+L + EL+E A  +   F++EASVGGAMPIIN A   LAGN I S+ GILNG
Sbjct: 121 VTSNKGPLSLYFSELVETANSNNAEFKYEASVGGAMPIINFAHNNLAGNNISSVLGILNG 180

Query: 179 TTNYILTKMEKEGLDFETALKEAKELGIAETDPTQDIEGLDTAAKIVILANSIMGMNKTI 238
           TTNYIL++M  EG  +E  LKEA+ELGIAETDPTQD+EG+D AAKIVILANS++  N TI
Sbjct: 181 TTNYILSRMANEGSSYEQTLKEAQELGIAETDPTQDVEGIDAAAKIVILANSVLNRNVTI 240

Query: 239 KDVKVKGISRITPEALFLANKRGYTIKLIGQIKDGYLIVEPMLVPIDSPLNVKGTLNVAM 298
           KDV ++GI+ ITPE++ LA K G+ IKLIG+  +  L V P LV   SP  V GTLNVA 
Sbjct: 241 KDVHMEGITNITPESIELAKKEGFLIKLIGEASNNNLEVAPRLVKEGSPFAVDGTLNVAT 300

Query: 299 FETDLAKEVVVVGRGAGPIETASAILSDLIHIYNS 333
             TDLA +V VVG+GAG IETASAILSD+I +  S
Sbjct: 301 VMTDLADDVTVVGKGAGSIETASAILSDIICVKKS 335


Lambda     K      H
   0.314    0.135    0.366 

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: 374
Number of extensions: 20
Number of successful extensions: 3
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: 336
Length of database: 339
Length adjustment: 28
Effective length of query: 308
Effective length of database: 311
Effective search space:    95788
Effective search space used:    95788
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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