GapMind for Amino acid biosynthesis

 

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

Align N-succinyldiaminopimelate-aminotransferase (EC 2.6.1.17) (characterized)
to candidate WP_007472961.1 CMTB2_RS00510 hypothetical protein

Query= metacyc::MONOMER-6501
         (397 letters)



>NCBI__GCF_000170735.1:WP_007472961.1
          Length = 363

 Score =  213 bits (542), Expect = 7e-60
 Identities = 139/379 (36%), Positives = 204/379 (53%), Gaps = 24/379 (6%)

Query: 11  YPFEKLRALLADAGKPTHDLPPINLSIGEPKHAAPACVGQAIAANLAGLSVYPSTKGEPA 70
           YPFEKL  LL D   P      I+L+IGEP+   P  +   +  N+  L+ YP T GE  
Sbjct: 5   YPFEKLNELLKDIPHPDE---VISLTIGEPQFETPKFIQDELCKNVKYLNKYPKTAGEEV 61

Query: 71  LRQAISQWLSRRYSIPAPDPESEVLPVLGSREALFAFAQTVIDPSAGALVVCPNPFYQIY 130
           L++A   ++ RRY+I     + E+LP  G+RE LF F    + P   A    PNPFYQIY
Sbjct: 62  LKKAQRDFVKRRYNIELE--KDELLPSFGTRELLFNFP-LFLKPKKTAF---PNPFYQIY 115

Query: 131 EGAALLAGATPYYVNADPARDFGLRTGRVPDEVWRRTQLVFVCSPGNPAGNVMSLEEWRT 190
           EGAA+ A +   Y+      +F      +P ++      V + SP NP  +VM ++    
Sbjct: 116 EGAAIAANSKINYMPLKKENNFL----SIPSQLDGDEDFVILNSPNNPTASVMDIDLLCE 171

Query: 191 LFELSDRHGFVIAAYECYSEIYLDEDTPPLGSLQAARRLGRDRYTNLVAFSSLSKRSNVP 250
             E + +  FVI + ECYSEIY D+  P +  L+A+ R+G   + N++A +S+SKRS+ P
Sbjct: 172 WVEEALKKDFVILSDECYSEIYFDKKPPSI--LEASIRVGNKNFKNVLAINSISKRSSAP 229

Query: 251 GMRSGFVAGDAALLARFLLYRTYHGSAMSPVVSAASIAAWSMRRMCRKTAQYRAKFEAVL 310
           G+RSGF+AGD+ +L ++L +RTY G A    +  A+  AW           +R K++   
Sbjct: 230 GLRSGFIAGDSKILKKYLNFRTYVGCASPLPLQYAAAKAWMDD---EHVETFREKYKRNF 286

Query: 311 PILQNVLDVRAPQASFYLWAGTPGSDTAFARELYGRTGVTVLPGSLLAREAHNANPGQGR 370
            I + +L +  P+A+FY+W      D  F +E Y R GV V+PG  + RE      G G 
Sbjct: 287 EIAKEILGIEVPKATFYIWLEV-DDDIEFTKEAYKR-GVKVMPGRFMGREGE----GVGY 340

Query: 371 IRIALVAPLDQCVQAAERI 389
           IRIALV   ++  QA + I
Sbjct: 341 IRIALVYNEEKTKQALKII 359


Lambda     K      H
   0.321    0.135    0.412 

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: 347
Number of extensions: 18
Number of successful extensions: 7
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: 397
Length of database: 363
Length adjustment: 30
Effective length of query: 367
Effective length of database: 333
Effective search space:   122211
Effective search space used:   122211
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 50 (23.9 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