GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Desulfovibrio vulgaris Miyazaki F

Align succinyldiaminopimelate transaminase (EC 2.6.1.17) (characterized)
to candidate 8500823 DvMF_1564 aminotransferase class I and II (RefSeq)

Query= BRENDA::P9WPZ5
         (397 letters)



>FitnessBrowser__Miya:8500823
          Length = 400

 Score =  155 bits (392), Expect = 2e-42
 Identities = 115/362 (31%), Positives = 171/362 (47%), Gaps = 25/362 (6%)

Query: 5   RLRPYATTVFAEMSALATRIGA-VNLGQGFPDEDGPPKMLQAAQDAIAGG--VNQYPPGP 61
           R+R    +    M  LA ++G  V+LGQG P    P  +++A   A+       +Y   P
Sbjct: 16  RVRNIRISATKLMPMLAAKVGGCVSLGQGVPSFRTPDHIVEAVCRALRDDPTAGRYSLQP 75

Query: 62  GSAPLRRAIAAQRRRHFGVDYDPETEVLVTVGATEAIAAAVLGLVEPGSEVLLIEPFYDS 121
           G   LR AIAA      G  +DPETE+ VTVGA EA+   +L +VE G EV++  P Y S
Sbjct: 76  GMPALREAIAADILARKGARFDPETEIGVTVGAMEALVMIMLTVVERGDEVIIPSPGYAS 135

Query: 122 YSPVVAMAGAHRVTVPLVPDGRGFALDADALRRAVTPRTRALIINSPHNPTGAVLSATEL 181
           ++  V MA    V VPL      + LD +A+R AVTPRTRA+I+ SP NPTG V    ++
Sbjct: 136 HAEQVLMAEGVPVHVPL--RAADWGLDVEAVRFAVTPRTRAIIVCSPGNPTGGVYDDADV 193

Query: 182 AAIAEIAVAANLVVITDEVYEHLVFDHARHLPL---AGFDGMAERTITISSAAKMFNCTG 238
            A+ ++A+  +LV+I D+ Y+++V+      P         +    IT++S +K +  TG
Sbjct: 194 RALCDLALERDLVLIVDDTYDYMVYGEQPGTPRFSPVSQPELRRHVITVNSFSKKYALTG 253

Query: 239 WKIGWACGPAELIAGVRAAKQYLSYVGGAPFQPAVALALDTEDAWVAALRNSLRARRDRL 298
           W++G+    A  +A +       +       Q A   AL      V  +R +L ARRD  
Sbjct: 254 WRVGYVAADAAWMAELLKVHDATAVCAPTVSQHAALAALTGPQDCVDVMRAALTARRDLT 313

Query: 299 AAGLTEIGFAVHDSYGTYFLCADPRPLGY---------DDSTEFCAALPEKVGVAAIPMS 349
              L        D+   +F    PR   Y          DS      + E+  V  +P  
Sbjct: 314 CRRL--------DALAPHFAYVPPRGAFYAMARYTFTDADSMTVARRMLEEARVITVPGG 365

Query: 350 AF 351
           +F
Sbjct: 366 SF 367


Lambda     K      H
   0.321    0.135    0.405 

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: 457
Number of extensions: 27
Number of successful extensions: 4
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: 400
Length adjustment: 31
Effective length of query: 366
Effective length of database: 369
Effective search space:   135054
Effective search space used:   135054
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