GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Azospirillum brasilense Sp245

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate AZOBR_RS05495 AZOBR_RS05495 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>FitnessBrowser__azobra:AZOBR_RS05495
          Length = 381

 Score =  299 bits (766), Expect = 1e-85
 Identities = 162/366 (44%), Positives = 223/366 (60%), Gaps = 3/366 (0%)

Query: 16  IFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIAREEL 75
           I DTTLRDGEQT GVA T +EK+ IAR LDE GV  +E G  A    E + IR +A   L
Sbjct: 9   INDTTLRDGEQTAGVAFTLDEKIAIARALDEAGVPELEIGIPAMGPEEREGIRAVAALGL 68

Query: 76  DAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVVEYAR 135
            A +    RM   D+ AA++ +   V++ +P S++H+ KKL+  R   L      V+ AR
Sbjct: 69  KARLMVWCRMHDTDLKAALDCKVGTVNLSMPVSDIHITKKLKRSRAWALAEIERKVKTAR 128

Query: 136 DHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKKLRER 195
           DHGL V +  ED +R ++++L        EAGA R  + DT+GV+ P      +++LR  
Sbjct: 129 DHGLEVSLGGEDSSRADMDFLIAAATVAQEAGARRFRFADTLGVLDPFQTRACIERLRRA 188

Query: 196 VGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVLEELY 255
              D+ + +H HDD G+A AN++AAV  GA  V+ TVNG+GERAGNA LEEVVV L+ LY
Sbjct: 189 T--DLEIEIHAHDDLGLANANSLAAVLGGATHVNTTVNGLGERAGNAPLEEVVVSLKVLY 246

Query: 256 GVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTYEPIP 315
           G D G+ T  L  +S LVER +   V  NK++VG+  FTHE+GIH DG+L+D +TY+   
Sbjct: 247 GQDCGVDTRALGAISDLVERASNRPVAVNKSIVGDAVFTHEAGIHVDGLLRDRATYQNFD 306

Query: 316 PEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKRI-TEADL 374
           P +VG E R VLGKH GT+ ++    Q+G+  DD     +L R++ L  R KR  T  +L
Sbjct: 307 PAEVGREHRIVLGKHSGTAGVKMAYGQLGIPCDDATAQAVLPRVRALATRAKRAPTAEEL 366

Query: 375 RAIAED 380
           RA  +D
Sbjct: 367 RAFHDD 372


Lambda     K      H
   0.315    0.134    0.367 

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: 480
Number of extensions: 18
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: 509
Length of database: 381
Length adjustment: 32
Effective length of query: 477
Effective length of database: 349
Effective search space:   166473
Effective search space used:   166473
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 Apr 09 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