GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Ammonifex degensii KC4

Align homoserine dehydrogenase (EC 1.1.1.3) (characterized)
to candidate WP_015738897.1 ADEG_RS04485 homoserine dehydrogenase

Query= BRENDA::D8WXQ1
         (432 letters)



>NCBI__GCF_000024605.1:WP_015738897.1
          Length = 427

 Score =  383 bits (984), Expect = e-111
 Identities = 204/423 (48%), Positives = 288/423 (68%), Gaps = 5/423 (1%)

Query: 1   MEAIQVGLLGLGTVGSGVVKIIENHQDKLMHQVGCPVKVKKILVQDLNKKRDVDVDPAQL 60
           M +  +GLLGLGTVG GV ++++ + + +  ++G  ++V KILV+D  K R + V P  L
Sbjct: 1   MRSFGIGLLGLGTVGRGVYRVLQENGEIIASRLGARLEVVKILVRDPKKDRGLAVPPELL 60

Query: 61  TTNADDILQDPDIDVVIEVMGGIEETRNYLLKALSEKKHVVTANKDLMAVYGSELLTAAS 120
           TT+  +++  P +D+V+EVMGG+E  R Y+L+AL + K VVTANKDL+A++G EL   AS
Sbjct: 61  TTDPQEVISHPAVDIVVEVMGGVEPARRYVLQALEQGKMVVTANKDLLALHGRELFDVAS 120

Query: 121 ANGCDLFYEASVAGGIPILRSLVDGLASDRITKMMGIVNGTTNYILTKMSKHGRAYEEVL 180
           A   DLF+EASVAGGIPI++ L + LA++RI +++GI+NGTTNYILT+MS+ G  +   L
Sbjct: 121 AARTDLFFEASVAGGIPIIKILKESLAANRIREIIGIINGTTNYILTRMSEEGLDFALAL 180

Query: 181 KEAQELGYAEADPASDVEGLDAARKMAILATLGFSMKIDLDDVKVEGITRITEEDIQYGK 240
            EAQ+ GYAEADP +D+EGLDAARK+AILA++ F+ ++   +V  EGI+RI   DI+Y +
Sbjct: 181 SEAQKHGYAEADPRADIEGLDAARKIAILASIAFNSRVTFPEVYAEGISRIEPADIKYAR 240

Query: 241 QLGYTMKLIGIAHREGEKVEVSVQPTLLSDSHPLASVNDEYNAVYVYGEAVGETMFYGPG 300
           +LGYT+KL+ +A    + +EV V P L+S  HPLASV D +NAV+V G+AVGETMFYG G
Sbjct: 241 ELGYTIKLLALARETEKGLEVRVHPALVSFKHPLASVRDVFNAVFVRGDAVGETMFYGRG 300

Query: 301 AGSLPTATAVVSDLVGVMKNMRLGVNGANAVTPQYQKKLKGPDEIYSKFFLRLHVKDEVG 360
           AG LPTA+AVV D++   + +  GV G    T   QK L   +E  S F+LR+   D  G
Sbjct: 301 AGELPTASAVVGDIMTAARQLLHGVKGMWGCTCFEQKPLVPVEETESCFYLRIKAVDRPG 360

Query: 361 VFANITSIFSEHSVSFEKILQMPLKENGLAEIVLVTH---QASLQDYEDILVKLRDLNAV 417
           V A I   F  H VS   ++Q    E  +A++VLVTH   +A+L+  E+ L KL  + AV
Sbjct: 361 VLAGIAGAFGRHEVSLAAVIQKTTGE--VADLVLVTHRVKEANLRAAEEELKKLPTVEAV 418

Query: 418 HEI 420
             +
Sbjct: 419 ANV 421


Lambda     K      H
   0.316    0.134    0.368 

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: 483
Number of extensions: 19
Number of successful extensions: 3
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: 432
Length of database: 427
Length adjustment: 32
Effective length of query: 400
Effective length of database: 395
Effective search space:   158000
Effective search space used:   158000
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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