GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapE in Pseudomonas putida KT2440

Align Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; EC 3.5.1.18; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase (uncharacterized)
to candidate PP_3571 PP_3571 putative Acetylornithine deacetylase

Query= curated2:Q3J9B0
         (376 letters)



>FitnessBrowser__Putida:PP_3571
          Length = 391

 Score =  102 bits (253), Expect = 2e-26
 Identities = 117/399 (29%), Positives = 162/399 (40%), Gaps = 48/399 (12%)

Query: 3   ATLELAKRLIACASITPRDAGCQ--GLLAQRLLALGFQGEQMNFGEVDNIWLRRGQKPPL 60
           A+  L  RLI  A+++ RD+     G +   L  LG + E  +  E        G K  L
Sbjct: 10  ASRALLARLIGFATVS-RDSNLALIGFIRDYLAELGVECELFHNPE--------GTKANL 60

Query: 61  F-----------VFAGHTDVVPPGPPDKWLTDPFTPEVRNGLLYGRGAADMKGSLAAMVT 109
           F           V +GHTDVVP      W  +PF    R+G LYGRG ADMKG +A+++ 
Sbjct: 61  FATVGPRDVGGVVLSGHTDVVPVDG-QAWTVEPFALSERDGRLYGRGTADMKGFIASVLA 119

Query: 110 ACEHFINVHSDHAGSIAFLLTSDEEGPAINGTIKVVETLQARGEKIDYCLVGEPTSQKQV 169
           A   F+         +AF  + DEE   + G   ++  LQ R  K   CL+GEPT  K V
Sbjct: 120 AVPAFLAQPLRMPVHLAF--SYDEEVGCL-GVRSMLAALQQRPCKPRLCLIGEPTELKPV 176

Query: 170 GDMIKNGRRGSLGGRLIVRGIQGHVAYPHLADNPIHSLAPALA-------VLCAQTWDQG 222
                 G +G L  R  V+G   H AY     N I   A  +         L        
Sbjct: 177 -----LGHKGKLAMRCQVQGAACHSAYAPYGVNAIEYAAKLIGKLGEIGEALALPVHHDE 231

Query: 223 NKDFPPTTFQISNIQGGTGATNVIPGEVEILFNFR----YSTEVTHQQLQQQMEEILSQQ 278
             D P +T Q   I+GG  A N++P E E  F  R    +  +    QLQ   E  L  +
Sbjct: 232 RFDPPFSTVQAGVIKGGR-ALNIVPDECEFDFEVRALPGFEAQAVADQLQTYAEAELLPR 290

Query: 279 RLNYELEWTLSGKPFLTAPGSLMTAVSQAVRGI---TGIDAEFSTTGGTSDGRFIAPTGA 335
                    +   P    PG      S+A R +   +G D  F T    ++G      G 
Sbjct: 291 MRKVNTASAIRLAPLSAYPGLATPEDSEAARLVALLSGSDT-FGTVAFGTEGGLFDQAGI 349

Query: 336 QVVELGPVNATI-HKVNECVAVADLEILSRIYSRILEIL 373
             V  GP +    HK +E V+V  L     +  R+++ L
Sbjct: 350 PTVVCGPGSMDQGHKPDEFVSVEQLRGCDAMLLRLVDYL 388


Lambda     K      H
   0.319    0.136    0.406 

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: 352
Number of extensions: 20
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: 376
Length of database: 391
Length adjustment: 30
Effective length of query: 346
Effective length of database: 361
Effective search space:   124906
Effective search space used:   124906
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 (21.7 bits)
S2: 50 (23.9 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