GapMind for Amino acid biosynthesis

 

Alignments for a candidate for pre-dehydr in Desulfovibrio gracilis DSM 16080

Align prephenate dehydrogenase (EC 1.3.1.12); prephenate dehydratase (EC 4.2.1.51); chorismate mutase (EC 5.4.99.5) (characterized)
to candidate WP_078715825.1 B5D49_RS01230 prephenate dehydratase

Query= BRENDA::O30012
         (620 letters)



>NCBI__GCF_900167125.1:WP_078715825.1
          Length = 372

 Score =  147 bits (370), Expect = 1e-39
 Identities = 105/330 (31%), Positives = 168/330 (50%), Gaps = 13/330 (3%)

Query: 269 LRGLIKSIDSLILRLIERRIDAARQIARIKMERGEPIELKDVEEEKLW--EVMSKTTLNP 326
           +R  I ++D  IL L+ +R + + ++ R K    EPI     E+E +   +V++   L  
Sbjct: 18  MRERIDALDEAILDLLNQRAEVSLEVGRHKAGSAEPIFKPRREKEVITRLQVLNPGPLPD 77

Query: 327 VKLKEIFEGIMSLAKEEEYKVAGVKYTIAVLGPQGSFSEEMALKLVGSRVPLRYCSTTDE 386
             L  I+  IMS ++  +         +  LGP+G+FS    ++ +G    L   S   E
Sbjct: 78  RHLYSIYREIMSSSRRLQRPER-----VVYLGPEGTFSYFAGIEFMGHMAELTPKSNLGE 132

Query: 387 IIKLVESGEVDYGLVPIENSVNGTVLPVIDALLNHDVEVFGEAKLEVNHCLVAKRKIELK 446
           + + V  G  + G+VP+ENS+ GTV   +D  + + V V  E    ++H L+A     L 
Sbjct: 133 VFRAVAEGGAELGIVPLENSLQGTVGQTVDLFMRYPVFVQAELYSRISHALLAAVP-GLG 191

Query: 447 EIKTIYSHPQAVAQCMGFINNYLPSVAIRYTTSTSDAARM---LDDYSAAIMSENAARFY 503
            +  +YSH +A+ QC  ++   LP       +ST+ AAR+     D SA +     A  +
Sbjct: 192 HVTRVYSHSKALGQCGEWLEANLPEAPRLPMSSTAAAARLARDAGDGSAVVGHVRLAELF 251

Query: 504 RLHVLRKGIQDLKGRNITRFYLIRRRSGR-SEGKITSLFFGVEDKPGALKDVLEVFHKKG 562
            L+VL + ++DL   N TRF +I    G+  E   +S+ F   D+PGAL  VLE+F ++G
Sbjct: 252 GLNVLAEHLEDLPD-NWTRFLVIAPAPGQEKERDKSSILFTTPDRPGALGTVLEIFSRRG 310

Query: 563 FNLRKLESRPAGTGLGDYVFFVEVEAPLRE 592
            NL KLESRP+      YVFF ++E  L +
Sbjct: 311 VNLSKLESRPSRGERWKYVFFADLECDLAD 340


Lambda     K      H
   0.320    0.137    0.380 

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: 424
Number of extensions: 18
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: 620
Length of database: 372
Length adjustment: 34
Effective length of query: 586
Effective length of database: 338
Effective search space:   198068
Effective search space used:   198068
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: 51 (24.3 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