GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Thermodesulforhabdus norvegica DSM 9990

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_093396405.1 BM091_RS13065 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_900114975.1:WP_093396405.1
          Length = 388

 Score =  412 bits (1059), Expect = e-120
 Identities = 190/386 (49%), Positives = 267/386 (69%)

Query: 6   ITPADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPK 65
           I  A+R+++LPPY+F  LD L+ + R QG+D+ID G+G+PD  TP  +V+A  +A++DP 
Sbjct: 3   IERAERLKKLPPYLFKELDRLRDEVRAQGVDIIDFGVGDPDLPTPDHIVEALKKAVEDPS 62

Query: 66  NHGYPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVL 125
            H YP + G   FR  +  WY +R+GV LDP  E + L+GSKEG++H+ +A++NPGD+ L
Sbjct: 63  THRYPSYSGMNDFRDCVARWYKKRFGVDLDPAREVIVLIGSKEGIAHIPLAFINPGDLAL 122

Query: 126 VPSPAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGA 185
           VP+PAYP +  G + AGG  + + L  END+L DL AIPE+VA KA++++ NYP+NPT A
Sbjct: 123 VPTPAYPVYHTGTIFAGGESYFMPLLEENDFLPDLNAIPEDVAEKARMMFINYPNNPTSA 182

Query: 186 TAPREFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTY 245
            A  +FF  +V FAR Y I++ HD  Y+ELAFDGY+P S L++ GAK++G+EFH+LSKTY
Sbjct: 183 VAEEDFFRRVVDFARTYNIIVCHDAAYSELAFDGYKPMSFLQVEGAKEVGIEFHSLSKTY 242

Query: 246 NMAGWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTR 305
           NM GWR+GF VGN  VIQGL  +K+N+D G F A+Q A   AL+     + E  + Y+ R
Sbjct: 243 NMTGWRLGFAVGNAEVIQGLGQVKSNIDSGAFNAVQMAGIAALEGDQTCVEENCRIYKER 302

Query: 306 RDFLIQGLGELGWDVPKTKATMYLWVKCPVGMGSTDFALNLLQQTGVVVTPGNAFGVAGE 365
           RD L+ GL   G      KAT Y+W + P    STDF++ LL++ G+V TPGN FG  GE
Sbjct: 303 RDVLVAGLRSAGLKPIVPKATFYVWCRIPENTTSTDFSMRLLKEAGIVTTPGNGFGEPGE 362

Query: 366 GYVRISLIADCDRLGEALDRIKQAGI 391
           GYVR +L    +R+ EA++RIK+ G+
Sbjct: 363 GYVRFALTVPVERIEEAIERIKKLGV 388


Lambda     K      H
   0.321    0.140    0.427 

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: 490
Number of extensions: 21
Number of successful extensions: 1
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: 403
Length of database: 388
Length adjustment: 31
Effective length of query: 372
Effective length of database: 357
Effective search space:   132804
Effective search space used:   132804
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