GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Azospirillum sp. B510

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_012973278.1 AZL_RS03450 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000010725.1:WP_012973278.1
          Length = 377

 Score =  288 bits (736), Expect = 3e-82
 Identities = 157/374 (41%), Positives = 219/374 (58%), Gaps = 3/374 (0%)

Query: 10  PPDEVRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRR 69
           P     I DTTLRDGEQT GVA T +EK+ IA+ LD  GV   E G  A  E E + IR 
Sbjct: 2   PTTFATINDTTLRDGEQTAGVAFTLDEKIAIAKALDAAGVPEQEIGIPAMGEEEREGIRA 61

Query: 70  IAREELDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERARE 129
           +A   L   +    RM   D+ AA+  +   V++ +P S++H+ +KL+  R   L     
Sbjct: 62  VAALGLKGRLMVWCRMHDTDLKAALSCDVGFVNLSMPVSDIHITRKLKRSRAWALAEIER 121

Query: 130 VVEYARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAV 189
            V+ ARDHGL V +  ED +R ++++L         AGA R  + DT+GV+ P      +
Sbjct: 122 RVKQARDHGLEVSVGGEDSSRADMDFLIAAASVAQAAGARRFRFADTLGVLDPFQTRACI 181

Query: 190 KKLRERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVV 249
           ++LR     D+ + +H HDD G+A AN++AAV  GA  V+ TVNG+GERAGNA LEEVVV
Sbjct: 182 ERLRRAT--DLEIEIHAHDDLGLANANSLAAVLGGATHVNTTVNGLGERAGNAPLEEVVV 239

Query: 250 VLEELYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDES 309
            L+ LY +D+G+ T  L  +S LVER +   V  NK++VG   FTHE+GIH DG+L+D +
Sbjct: 240 SLKHLYHIDSGVETRSLGAISDLVERASNRPVAVNKSIVGAAVFTHEAGIHVDGLLRDRA 299

Query: 310 TYEPIPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKR- 368
           TY+   P +VG E R VLGKH GT+ ++   + +G+  DD     +L R++ L  R KR 
Sbjct: 300 TYQNFDPAEVGREHRIVLGKHSGTAAVKLAYEGLGIACDDSMAQAVLPRVRALATRAKRP 359

Query: 369 ITEADLRAIAEDVL 382
            T  +L A  E  L
Sbjct: 360 PTPEELHAFLEACL 373


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: 488
Number of extensions: 20
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: 377
Length adjustment: 32
Effective length of query: 477
Effective length of database: 345
Effective search space:   164565
Effective search space used:   164565
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.

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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