GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Dinoroseobacter shibae DFL-12

Align N-succinyldiaminopimelate-aminotransferase (EC 2.6.1.17) (characterized)
to candidate 3606628 Dshi_0060 aminotransferase class I and II (RefSeq)

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



>FitnessBrowser__Dino:3606628
          Length = 393

 Score =  243 bits (619), Expect = 9e-69
 Identities = 153/378 (40%), Positives = 199/378 (52%), Gaps = 12/378 (3%)

Query: 4   RLDALHPYPFEKLRALLADAGKPTHDLPPINLSIGEPKHAAPACVGQAIAANLAGLSVYP 63
           R  AL  Y F +LRALL D   P      + +SIGEP+H  P     A+A  L   + YP
Sbjct: 6   RFSALPEYAFPRLRALL-DGHPPGGST--LAMSIGEPQHPFPQIATDALAEALPLFNKYP 62

Query: 64  STKGEPALRQAISQWLSRRYSIPAPDPESEVLPVLGSREALFAFAQTVI-DPSAGA--LV 120
              G P L  AI+ W+  RY +   DP  +VL + G+RE LFA    +  D  AG   LV
Sbjct: 63  PNDGAPELCAAIADWVQGRYGVKL-DPARQVLALNGTREGLFAACLALCPDTKAGGQPLV 121

Query: 121 VCPNPFYQIYEGAALLAGATPYYVNADPARDFGLRTGRVPDEVWRRTQLVFVCSPGNPAG 180
             PNPFYQ+Y   A  AGA P +VNA     F      +P E   R  + +VCSP NP G
Sbjct: 122 AMPNPFYQVYAVGAQAAGARPLFVNATAETGFLPNLTTLPPETLDRIAIAYVCSPSNPQG 181

Query: 181 NVMSLEEWRTLFELSDRHGFVIAAYECYSEIYLDEDTPPLGSLQAARRLGRDRYTNLVAF 240
            V     WR L  L+++H F + A ECY+EIY   +TPP G+L+ A  +G D    +V F
Sbjct: 182 AVADAGYWRALIGLAEKHDFYVFADECYAEIY--RETPPCGALEIATAMGADP-ERVVIF 238

Query: 241 SSLSKRSNVPGMRSGFVAGDAALLARFLLYRTYHGSAMSPVVSAASIAAW-SMRRMCRKT 299
            SLSKRSN+PG+RSGF AG    +A     R Y G+ +   +   + A W     +    
Sbjct: 239 HSLSKRSNLPGLRSGFAAGGPRAMAEMKKLRAYAGAPLPGPLHPVATAVWRDEAHVVENR 298

Query: 300 AQYRAKFEAVLPILQNVLDVRAPQASFYLWAGTPGSDTAFARELYGRTGVTVLPGSLLAR 359
           A Y AKF+    IL  V    +P A F+LW      + A A +L+  TGV VLPG+ L+R
Sbjct: 299 ALYAAKFDTADTILGAVPGYTSPAAGFFLWLPVEDGEAA-ALKLWTETGVRVLPGAYLSR 357

Query: 360 EAHNANPGQGRIRIALVA 377
           +    NPG G IR+ALVA
Sbjct: 358 DTETGNPGAGFIRVALVA 375


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: 532
Number of extensions: 24
Number of successful extensions: 8
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: 393
Length adjustment: 31
Effective length of query: 366
Effective length of database: 362
Effective search space:   132492
Effective search space used:   132492
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 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