Aligments for a candidate for lysT in Caulobacter crescentus NA1000

GapMind for Amino acid biosynthesis

Aligments for a candidate for lysT in Caulobacter crescentus NA1000

Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate CCNA_00196 CCNA_00196 3-isopropylmalate dehydratase large subunit

Query= curated2:O27668
         (428 letters)



>lcl|FitnessBrowser__Caulo:CCNA_00196 CCNA_00196 3-isopropylmalate
           dehydratase large subunit
          Length = 479

 Score =  202 bits (514), Expect = 2e-56
 Identities = 148/447 (33%), Positives = 213/447 (47%), Gaps = 69/447 (15%)

Query: 30  VDLAMTHDGTSPPTIRTFRDIASRGGPARVWDPERIVMVFDHNVPANTIGAAEFQRVTRE 89
           +DL + H+ T+P   + F  + + G   R   P+R + V DHN+P     A     V  E
Sbjct: 27  IDLHLIHEVTTP---QAFAGLRAAGRKVR--RPDRTLAVADHNIPTEG-QALGVDAVADE 80

Query: 90  FAREQGIVNIFQNAA--------------GICHQVLPERGFVRPGMVIVGADSHTCTYGA 135
            AR Q +  + +N A              GI H V PE+G  +PGM IV  DSHT T+GA
Sbjct: 81  EARLQ-LKTLARNVADNGIEFFPMGDIRNGIVHVVGPEQGRTQPGMTIVCGDSHTSTHGA 139

Query: 136 FGAFATGMGATDMAMVFATGKTWFMVPEAMRIEVTGEPEGHVYAKDVILHIIGEIGVDGA 195
           FGA A G+G +++  V AT        + M + V G+    V  KDV L +IGEIG  G 
Sbjct: 140 FGALAHGIGTSEVEHVLATQTLRQKKAKNMLVRVDGQLPPGVTGKDVALAVIGEIGTAGG 199

Query: 196 TYRSVEFTGDTIESMDVSGRMTICNMAVEMGAKNGIMEPNRQTLDYVRARTG-------- 247
           T   +EF G+ I  + + GRMT+CN+ +E GAK G++ P+ +T  Y++ +          
Sbjct: 200 TGYVIEFAGEAIAGLSMEGRMTLCNLTIEGGAKAGLVAPDDKTFAYIQGKPAAPKGAAWD 259

Query: 248 ---REFRVYSSDEDSQYLEDHHFDVSDLEPQVACPDDVDNVYPV---------------- 288
                ++ + +DED+ +      D S L P V      ++V PV                
Sbjct: 260 MALSHWKTFFTDEDAVFDRTVVIDGSALVPMVTWGTSPEDVIPVTGNVPDPESFATPDKR 319

Query: 289 ---HR------------VEGTHIDEAFLGSCTNGRYEDLKIAAEVIGD-----RRVHEDV 328
              HR            +    ID  F+GSCTN R ED++ AA V+ +     R V   V
Sbjct: 320 AAAHRALDYMGLKAGQPISEARIDRVFIGSCTNSRIEDMRAAAAVVQEAFLHGRLVAPHV 379

Query: 329 RFIVSPASREIYLKALEDGIIETFIRAGAIVCNPGCGPCLGAHMGVLAPGEVSIATTNRN 388
           + +V P S  +  +A E+G+   F  AG     PGC  CL  +   LAP E   +T+NRN
Sbjct: 380 KAMVVPGSGLVKEQAEEEGLDAIFKAAGFDWREPGCSMCLAMNPDKLAPQERCASTSNRN 439

Query: 389 FRGRMGDPASSVYLANPAVVAESAIEG 415
           F GR G  A   +L +PA+ A +AI G
Sbjct: 440 FEGRQG-RAGRTHLVSPAMAAAAAIAG 465



 Score = 24.3 bits (51), Expect = 0.009
 Identities = 17/54 (31%), Positives = 26/54 (48%)

Query: 371 HMGVLAPGEVSIATTNRNFRGRMGDPASSVYLANPAVVAESAIEGVISAPQQEA 424
           +MG+ A   +S A  +R F G   +       A  AVV E+ + G + AP  +A
Sbjct: 328 YMGLKAGQPISEARIDRVFIGSCTNSRIEDMRAAAAVVQEAFLHGRLVAPHVKA 381


Lambda     K      H
   0.320    0.137    0.408 

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: 577
Number of extensions: 39
Number of successful extensions: 6
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: 428
Length of database: 479
Length adjustment: 33
Effective length of query: 395
Effective length of database: 446
Effective search space:   176170
Effective search space used:   176170
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 (21.8 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.

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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:

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, or view the source code, or see 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