GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Azorhizobium caulinodans ORS 571

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_043879531.1 AZC_RS17440 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000010525.1:WP_043879531.1
          Length = 399

 Score =  263 bits (673), Expect = 7e-75
 Identities = 154/350 (44%), Positives = 200/350 (57%), Gaps = 2/350 (0%)

Query: 18  DTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIAREELDA 77
           DTTLRDGEQ PGVA T +EK+ IA  L   GV  IEAG  A  + E++ IR I    L  
Sbjct: 20  DTTLRDGEQAPGVAFTRKEKIEIAAALAAAGVPEIEAGTPAMGDEEVETIRSIVSLNLPT 79

Query: 78  EVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVVEYARDH 137
            V +  RM + D+ AAV A    V++ +PTS+  +  KL  DR   L R  EVV  AR  
Sbjct: 80  RVMAWCRMSEDDLMAAVAAGVKIVNVSIPTSDRQLAGKLGKDRAWALGRVAEVVTLARRL 139

Query: 138 GLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKKLRERVG 197
           G  V +  ED +R + ++L  + +    AGA RL   DT+GV+ P G +  V+++     
Sbjct: 140 GFEVAVGGEDSSRADPDFLCRLAETAKAAGAFRLRLADTLGVLDPFGTYALVRRVAATT- 198

Query: 198 EDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVLEELYGV 257
            D+ L  H HDD G+ATANT+AAV  GAR   VTV G+GERAGNAALEEV + L +    
Sbjct: 199 -DIELEFHAHDDLGLATANTLAAVMGGARHASVTVAGLGERAGNAALEEVAIALRQTARA 257

Query: 258 DTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTYEPIPPE 317
           +TGI    L  L++LV       VP  KA+VG + FTHESGIH  G+LKD +TYE + PE
Sbjct: 258 ETGIAPAALKPLAELVCGAAARPVPRGKAIVGADVFTHESGIHVSGLLKDRATYEALNPE 317

Query: 318 KVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGK 367
             G     VLGKH G + + K L   G+ VD  +   IL R++    R K
Sbjct: 318 LFGRGHTVVLGKHSGLAAVEKALADEGITVDAVRGRAILDRVRAFAVRTK 367


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: 453
Number of extensions: 21
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: 509
Length of database: 399
Length adjustment: 33
Effective length of query: 476
Effective length of database: 366
Effective search space:   174216
Effective search space used:   174216
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 10 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