GapMind for Amino acid biosynthesis

 

Alignments for a candidate for aro-dehydratase in Desulfobacter vibrioformis DSM 8776

Align arogenate dehydratase (EC 4.2.1.91) (characterized)
to candidate WP_035240982.1 Q366_RS16530 prephenate dehydratase

Query= BRENDA::Q9SA96
         (392 letters)



>NCBI__GCF_000745975.1:WP_035240982.1
          Length = 379

 Score =  140 bits (354), Expect = 5e-38
 Identities = 106/337 (31%), Positives = 163/337 (48%), Gaps = 26/337 (7%)

Query: 61  ELKKSSDELGLTQETQSLSFHRDLSMLPKPLTA-------NSLYSSDGDDSKVR-ISFQG 112
           E+KK      L +  + +   R     P P  A       N + ++  +  K R I F G
Sbjct: 52  EIKKQKGSQILDRSRERMVIERLSRTNPGPADASLIQYVFNVIITATREIQKPRTIGFLG 111

Query: 113 IPGAYSETAALKAFPNC-ETVPCEQFEAAFQAVELWLVDKAVLPIENSVGGSIHRNYDLL 171
              ++S  AAL  F +C E V    F   F  +E   +   ++P+ENS+ G+++   DL 
Sbjct: 112 PLASHSHIAALHYFRHCGEFVEQSGFFDIFNNIERKELHFGIVPVENSLEGAVNYTLDLF 171

Query: 172 LRHRLHIVQEVHLPVNHCLLGVPGVKKEDIKCVLSHPQALDQCVNSLNNLGIQRISAKDT 231
               +HI  E + PV+H LL + G  K D+K V SHPQA+ QC N L          + T
Sbjct: 172 AEFDIHITAEHYEPVSHDLLSITGELK-DVKTVYSHPQAIAQCKNWLKKHLPHATVMETT 230

Query: 232 ATAAQTVSSSGKIDVGAIASVRAANIYGLDILAENIQDDVNNVTRFLILAREPMIPRTDR 291
           +T+   + +S    + AIAS +AA+ Y L  +A  IQD   N+TRFL++      P    
Sbjct: 231 STSNAALMASKDEQIAAIASGKAAHFYTLLPVASKIQDRAGNITRFLVIGGNH--PERTG 288

Query: 292 PYKTSIVFSLEEGPGVLFKALAVFALRSINLSKIESRPQRRRPLRVVDGSNNGSAKYFDY 351
             KTSI+F+    PG LF+AL+      +N+ K+ESRP RR        SN      + Y
Sbjct: 289 NDKTSIMFATNHTPGALFRALSPVNRAGLNMVKLESRPTRR--------SN------WSY 334

Query: 352 LFYIDFEASMADTRAQHALGHLQEFASFIRILGCYPM 388
            F++D E  + D      +  ++  A ++++LG YP+
Sbjct: 335 HFFMDIEGHIQDEIVFQTIEQIRSQALYLKVLGSYPI 371


Lambda     K      H
   0.321    0.135    0.402 

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: 294
Number of extensions: 13
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: 392
Length of database: 379
Length adjustment: 30
Effective length of query: 362
Effective length of database: 349
Effective search space:   126338
Effective search space used:   126338
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 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