Alignments for a candidate for hom in Trichormus variabilis ATCC 29413

GapMind for Amino acid biosynthesis

Alignments for a candidate for hom in Trichormus variabilis ATCC 29413

Align homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized)
to candidate WP_011320349.1 AVA_RS18465 aspartate kinase

Query= BRENDA::Q9WZ17
         (739 letters)



>NCBI__GCF_000204075.1:WP_011320349.1
          Length = 604

 Score =  313 bits (802), Expect = 2e-89
 Identities = 172/419 (41%), Positives = 268/419 (63%), Gaps = 20/419 (4%)

Query: 339 SVVVMKFGGAAISDVEKLEKVAEKIIKRKKSGVKPVVVLSAMGDTTDHLIELAKTIDENP 398
           +++V KFGG+++  VE+++ VA+++ K  K+G   VVV+SAMG TTD L++LA  I  NP
Sbjct: 2   ALIVQKFGGSSVGSVERIQAVAQRVYKTVKAGNSLVVVVSAMGKTTDGLVKLANEISRNP 61

Query: 399 DPRELDLLLSTGEIQSVALMSIALRKRGYKAISFTGNQLKIITDKRYGSARIIDINTDII 458
           + RE+D+LLSTGE  ++AL+S+AL++ G  AIS TG Q+ I+T+  +  ARI+ I T+ +
Sbjct: 62  NRREMDMLLSTGEQVTIALLSMALQELGQPAISMTGAQVGIVTEAEHTRARILHIETERV 121

Query: 459 SRYLKQDFIPVVAGFQGITETG--DITTLGRGGSDLTAIALAYSLGADLCELYKDVDGVY 516
             ++++  + VVAGFQGI+  G  +ITTLGRGGSD +A+ALA +L AD CE+Y DV G+ 
Sbjct: 122 EGHIQEGKVVVVAGFQGISSNGSLEITTLGRGGSDTSAVALAAALQADFCEIYTDVPGIL 181

Query: 517 TADPRIVKDARVIKELSWEEMIELSRHGAQVLQARAAEFARKYGVKVLIKNAHKETRGTL 576
           T DPRIV +A+++ E++  EM+EL+  GA+VL  RA E AR YG+ +++K++  +  GT 
Sbjct: 182 TTDPRIVPEAQLMGEITCNEMLELASLGAKVLHPRAVEIARNYGMPLVVKSSWTDDPGTW 241

Query: 577 IW----EGTKVEN----PIVRAVTFEDGMAKVVLKDVPDKPGVAARIMRTLSQMGVNIDM 628
           +     +G  + N      V  V  +   AKV L  VPDKPGVAA++   +S+  V++D+
Sbjct: 242 VTTPKPQGRSLINLELARPVDDVELDTDQAKVALLRVPDKPGVAAKLFGEISRQKVDVDL 301

Query: 629 IIQGMKSGEYNTVAFIVPESQLGKLDI----------DLLKTRSEAKEIIIEKGLAKVSI 678
           IIQ +  G  N +AF V    L + +                +S+  E+++E+ +AKVSI
Sbjct: 302 IIQSIHEGNSNDIAFTVTTPILKRAEAVAAAIAPSLRSPSHPKSDEAEVMVEQNIAKVSI 361

Query: 679 VGVNLTSTPEISATLFETLANEGINIDMISASSSRISVIIDGKYVEDAVKAIHSRFELD 737
            G  +   P ++A +F TLA  G+NI MIS S  ++S +ID +  + A+ A+   FE++
Sbjct: 362 AGAGMIGRPGVAAKMFTTLAEAGVNIQMISTSEVKVSCVIDAQDGDRAIIALRKAFEIE 420



 Score = 92.4 bits (228), Expect = 6e-23
 Identities = 53/159 (33%), Positives = 88/159 (55%), Gaps = 7/159 (4%)

Query: 585 NPIVRAVTFEDGMAKVVLKDVPDKPGVAARIMRTLSQMGVNIDMIIQGMKSGEYNTV--- 641
           +P VR V  +   A++ ++ VPD+PG+AA++   L+Q  +++DMIIQ  +    + V   
Sbjct: 436 SPPVRGVALDLNQARLAIRQVPDRPGMAAQLFGILAQNNISVDMIIQSQRCRIVDGVPRR 495

Query: 642 --AFIVPESQLGKLDIDLLKTRSEAK--EIIIEKGLAKVSIVGVNLTSTPEISATLFETL 697
             AF VP          L +   E    +++++  +AKVSIVG  +   P ++A +FE L
Sbjct: 496 DIAFTVPRMDGETAQKLLCQVAPELGWGDVVLDSAIAKVSIVGAGMVGQPGVAAKMFEAL 555

Query: 698 ANEGINIDMISASSSRISVIIDGKYVEDAVKAIHSRFEL 736
           A   INI MI+ S  +IS ++  +    A++ IH+ FEL
Sbjct: 556 AKHQINIQMIATSEIKISCVVSQEQGVQALQVIHTAFEL 594


Lambda     K      H
   0.318    0.137    0.377 

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: 915
Number of extensions: 50
Number of successful extensions: 9
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 739
Length of database: 604
Length adjustment: 38
Effective length of query: 701
Effective length of database: 566
Effective search space:   396766
Effective search space used:   396766
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 (21.7 bits)
S2: 54 (25.4 bits)

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

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer
changes to Amino acid biosynthesis since the publication.

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

GapMind for Amino acid biosynthesis