GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Methanosarcina barkeri Fusaro

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (uncharacterized)
to candidate WP_011306884.1 MBAR_RS10080 homoserine dehydrogenase

Query= curated2:Q58997
         (336 letters)



>NCBI__GCF_000195895.1:WP_011306884.1
          Length = 331

 Score =  328 bits (842), Expect = 9e-95
 Identities = 174/329 (52%), Positives = 237/329 (72%), Gaps = 9/329 (2%)

Query: 5   IVGFGAIGKGIAKVLYDKKDYLKKNYEEFKVVAITDSSGAAIDEDGLDLLKAIEVK--EK 62
           I+GFGAIG+G+A+V   KK+YL+    E KVVA+ DS GA ++ +G+DL   +  K  ++
Sbjct: 8   ILGFGAIGQGVAEVFLMKKEYLESIGLEVKVVAVVDSKGATVNPEGVDLADCLVRKRRDR 67

Query: 63  TGKIKNYPEKGREMSSIDVIKEVDADVVVEVTPSNLETGDPAKTHILESFKNKKHVVTAN 122
           T  ++N       +S ++VI+ V  D+V+E TP+N+ TG     ++  +FK  K V+T+N
Sbjct: 68  TVALEN-------ISGVEVIQSVAHDLVIETTPTNILTGGAGMQNMFAAFKTGKDVITSN 120

Query: 123 KGPLALCYKELIEEAKKHGVIFRHEASVGGAMPIINLAKETLAGNEILSIRGILNGTTNY 182
           KGPL L Y+EL+E AK  G  FR EA+VGG+MPIINL  E LAGN++ SI+GILNGT NY
Sbjct: 121 KGPLTLKYRELMEAAKAAGSHFRFEATVGGSMPIINLVNEVLAGNKVKSIKGILNGTCNY 180

Query: 183 ILTKMEKEGLDFETALKEAKELGIAETDPTQDIEGLDTAAKIVILANSIMGMNKTIKDVK 242
           ILT+M +E   +   L E+ +LGIAETDPT D+EG+DTA K+VILAN+I G++ T  +V+
Sbjct: 181 ILTRMLEERASYNDILAESMQLGIAETDPTYDVEGIDTACKLVILANAIFGIDATYNNVE 240

Query: 243 VKGISRITPEALFLANKRGYTIKLIGQIKDGYLIVEPMLVPIDSPLNVKGTLNVAMFETD 302
           V GI+++TPEAL +A ++G+ IKLIG++    + V P LVPI+ PL V GTLNVA  ET+
Sbjct: 241 VTGITKVTPEALEMAYEKGHVIKLIGEVSRERIHVAPRLVPINHPLAVGGTLNVASVETE 300

Query: 303 LAKEVVVVGRGAGPIETASAILSDLIHIY 331
           LA E+ V G+GAGPIETASAILSDLI IY
Sbjct: 301 LAGEITVTGKGAGPIETASAILSDLIAIY 329


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: 339
Number of extensions: 12
Number of successful extensions: 2
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: 331
Length adjustment: 28
Effective length of query: 308
Effective length of database: 303
Effective search space:    93324
Effective search space used:    93324
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.

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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