GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Polaromonas naphthalenivorans CJ2

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_011801696.1 PNAP_RS11555 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000015505.1:WP_011801696.1
          Length = 395

 Score =  295 bits (756), Expect = 2e-84
 Identities = 164/374 (43%), Positives = 228/374 (60%), Gaps = 8/374 (2%)

Query: 11  PDEVRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRI 70
           P  + I DTTLRDGEQT GVA T +EK  IA  L   GV  +E G  A  E E+  I  I
Sbjct: 2   PLNLIINDTTLRDGEQTAGVAFTVDEKCAIACALAAAGVPEMEIGIPAMGEEEIDCINTI 61

Query: 71  AREELDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREV 130
           A  EL A +    R+   D+ +A+  +AD +H+ +P S++H++ KLR  RE VL +   V
Sbjct: 62  AALELPAALMIWGRLTDADLASALRCQADIIHLSIPVSDIHLRHKLRQSREWVLAQVTRV 121

Query: 131 VEYARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVK 190
           +E A   G  + +  ED +R +  +L +V     + GA R+ + DT+GV+ P   + A+ 
Sbjct: 122 IEKAVASGRKISLGAEDASRADAGFLSQVARRAQDCGASRIRFADTLGVLDPFTTYEAIT 181

Query: 191 KLRERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVV 250
           +LRE V  D+   +H H+D G+ATANT+AA+RAGA   + TVNG+GERAGNAALEEVV+ 
Sbjct: 182 RLREAVHLDI--EIHAHNDLGLATANTLAALRAGATHANTTVNGLGERAGNAALEEVVMG 239

Query: 251 LEELYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDEST 310
           +  L+   TG+ T+ L  +S+LV R +G +V  NK++VGE  FTHESGIH DG+LK+ ST
Sbjct: 240 VRHLHHAQTGVSTQALVSISRLVARASGRQVAFNKSIVGEAVFTHESGIHIDGLLKNAST 299

Query: 311 YEPIPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKRI- 369
           YE   P ++G ERR VLGKH G+  +R+    MGV +DD+ L    R L R+ D   R+ 
Sbjct: 300 YESFDPSELGRERRTVLGKHSGSQSVRQAYGAMGVVLDDDALTG--RVLARIRDHAMRVK 357

Query: 370 ---TEADLRAIAED 380
              T  +LR    D
Sbjct: 358 QEATPDELRGFLRD 371


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: 474
Number of extensions: 15
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: 395
Length adjustment: 33
Effective length of query: 476
Effective length of database: 362
Effective search space:   172312
Effective search space used:   172312
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