GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tpiA in Caminibacter mediatlanticus TB-2

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_007475101.1 CMTB2_RS07075 phosphoglycerate kinase

Query= BRENDA::P36204
         (654 letters)



>NCBI__GCF_000170735.1:WP_007475101.1
          Length = 404

 Score =  379 bits (973), Expect = e-109
 Identities = 199/387 (51%), Positives = 265/387 (68%), Gaps = 8/387 (2%)

Query: 12  KGKRVIMRVDFNVPVKD-GVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPKGEPSPE 70
           KG RV +R DFNVP+ + G + DD RIR ALPTIKY L+   K+++ SHLGRPKGE + +
Sbjct: 13  KGDRVFVRCDFNVPIDEFGNITDDRRIRMALPTIKYLLDNECKIVIASHLGRPKGEFNEK 72

Query: 71  FSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDPEL 130
           +SL PVAKRLS LL ++V     VVG + K     LK+GEVLLLEN RF   ETKND   
Sbjct: 73  YSLKPVAKRLSHLLKQDVIMANDVVGPDAKSKASNLKDGEVLLLENVRFDSRETKNDEGF 132

Query: 131 AKFWASLADIHVNDAFGTAHRAHASNVGIAQFIP---SVAGFLMEKEIKFLSKVTYNPEK 187
           AK  +   D ++NDAFG +HRAHAS   I +F       AGFL+ KEI F  K+  NP +
Sbjct: 133 AKELSEFGDFYINDAFGVSHRAHASVEAITRFYDECHKAAGFLLLKEINFFYKLLKNPVR 192

Query: 188 PYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAK 247
           P+V V+GG+KVS K+  + NL+ K D++++GG M FTFLKA+G  VG+S VE+D ID A 
Sbjct: 193 PFVAVVGGSKVSGKLQALINLLPKVDKMIVGGGMAFTFLKAMGYNVGNSLVEDDLIDEAL 252

Query: 248 ELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQK 307
           +++ +AK  GV+  LPVD VIA K       K V   + IP+GWMGLDIGP ++ LF + 
Sbjct: 253 KIMAEAKRLGVKFYLPVDIVIADKFSEDAIVKYVTYQE-IPDGWMGLDIGPASVRLFGEV 311

Query: 308 LSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDSAAAVNKFGLED 367
           L DA+T++WNGPMGV+E+D F+ GT +++  IA       I VVGGGD+A AV + G ++
Sbjct: 312 LWDAQTILWNGPMGVYEMDKFSRGTFKISHEIA---RSHGIKVVGGGDTADAVQRAGDDE 368

Query: 368 KFSHVSTGGGASLEFLEGKELPGIASI 394
           + + +STGGGASLE LEGK+LPG+A++
Sbjct: 369 EMTFISTGGGASLELLEGKKLPGVAAL 395


Lambda     K      H
   0.317    0.137    0.386 

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: 702
Number of extensions: 37
Number of successful extensions: 5
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: 654
Length of database: 404
Length adjustment: 35
Effective length of query: 619
Effective length of database: 369
Effective search space:   228411
Effective search space used:   228411
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: 52 (24.6 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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