GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Mesorhizobium ciceri WSM1271

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate YP_004143559.1 Mesci_4399 amidohydrolase

Query= curated2:Q04FS2
         (382 letters)



>NCBI__GCF_000185905.1:YP_004143559.1
          Length = 409

 Score =  206 bits (523), Expect = 1e-57
 Identities = 127/378 (33%), Positives = 200/378 (52%), Gaps = 18/378 (4%)

Query: 5   EQLIKIRRHLHANPEIGMQEVKTHQFLLEQIAKFPQENLTIETISEIPTALLVRIAGSDP 64
           +++I++RRHLH NPE+  QE  T ++L + +    Q  + I  ++    A+ +  AG   
Sbjct: 27  DRMIEVRRHLHRNPELSNQEAGTQRYLRQMLVD--QGIVDIRDVAGFGLAVDIVGAGRPS 84

Query: 65  KRTIALRTDMDALPIQEETGLDFASKNDHVMHACGHDIHMTVALGILSYFAKHQPKDN-- 122
            R IA+R D+DALPI+EE+G+D+AS N  VMHACGHD H ++A  + ++   HQ +D+  
Sbjct: 85  NRKIAIRADIDALPIEEESGVDYASTNPGVMHACGHDAHASMAFAVAAHL--HQSRDSFG 142

Query: 123 --LLVFFQPAEENE-FGGKRFYDAGGFQGEYLPDEFYALHVNPQLPAGQIASRKGTLFAG 179
             + + FQPAEE+E  GGKR  + G        D    +HV+P  P G+IA   G     
Sbjct: 143 GTVRLIFQPAEEDEPSGGKRVVEEGLLDDI---DAAICVHVDPYTPTGKIAVGSGPYTLA 199

Query: 180 SNELRISFIGKSGHAAYPQNAKDSIVAAANFVTNVQTVVSRNVDPIEGGVVTIGKFNAGK 239
            +   ++ IG + HAA P    D++  A + V+ +Q +VSR  DP +  V+++   N G 
Sbjct: 200 CDTFDVAVIGSAAHAAKPHEGVDALAVACSLVSELQKIVSRETDPYDPLVISVTAINGGN 259

Query: 240 AMNIIAGKADIEGTIRSFTQSGMEIMTKHIRMIAEGIAGAFGQELKINFRQGGYMPVVND 299
           A N+ AG+  ++GTIRS + +  E     +R IA G+A + G  ++++  + G   VVND
Sbjct: 260 AYNVTAGRVTLKGTIRSGSDATRERAWHRVRTIAAGMATSHGARVEVDIHK-GEPGVVND 318

Query: 300 ERTTNFFIDYMKNADGVDFKIVQPA-MIAEDFGFLSNQFEGTMCWLGVNDPK----HSLH 354
              T       K   G D  +  P   IA+DFG+ S +       LG+ + +      LH
Sbjct: 319 VEMTELIAASAKACIGADNVLNTPGWTIADDFGYYSEKRPSVYFRLGIRNEEIGSVFPLH 378

Query: 355 SDHLNPDESAITKGVEAI 372
                 DE+A+  G   +
Sbjct: 379 HARFRIDEAALKVGATTL 396


Lambda     K      H
   0.320    0.137    0.397 

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: 392
Number of extensions: 23
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: 382
Length of database: 409
Length adjustment: 31
Effective length of query: 351
Effective length of database: 378
Effective search space:   132678
Effective search space used:   132678
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 (21.8 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