GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Bacteroides thetaiotaomicron VPI-5482

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate 353461 BT3935 aminotransferase (NCBI ptt file)

Query= BRENDA::Q8YTF2
         (403 letters)



>FitnessBrowser__Btheta:353461
          Length = 393

 Score =  276 bits (705), Expect = 1e-78
 Identities = 143/384 (37%), Positives = 222/384 (57%), Gaps = 3/384 (0%)

Query: 6   ITPADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPK 65
           I PA+R+  +  Y F++  +  A+   +G D+I LG+G+PD    +  ++       DP 
Sbjct: 10  IAPAERLASVSEYYFSKKLKEVAQMNAEGKDVISLGIGSPDMPPSKVTIETLCNNAHDPN 69

Query: 66  NHGYPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVL 125
            HGY P+ G    R+    WY R YGV L+P++E  PL+GSKEG+ H+ +A+VNPG+ VL
Sbjct: 70  GHGYQPYVGIPELRKGFAAWYQRWYGVELNPNTEIQPLIGSKEGILHVTLAFVNPGEQVL 129

Query: 126 VPSPAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGA 185
           VP+P YP +     I G  V S  LK E+ W+ D  A+ +    + K+++ NYP+ PTGA
Sbjct: 130 VPNPGYPTYTSLSKILGAEVISYDLKEEDGWMPDFEALEKMDLNRVKLMWTNYPNMPTGA 189

Query: 186 TAPREFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTY 245
            A  E +E +V FAR+  I++V+D  Y+ +  +  +P S+L +PGAK+  +EF+++SK++
Sbjct: 190 NATPELYERLVDFARRKNIVIVNDNPYSFILNE--KPISILSVPGAKECCIEFNSMSKSH 247

Query: 246 NMAGWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTR 305
           NM GWR+G +  N   +Q +  +K+N+D G+F A+Q AA TAL+    +       YR R
Sbjct: 248 NMPGWRIGMLASNAEFVQWILKVKSNIDSGMFRAMQLAAATALEAEADWYEGNNHNYRGR 307

Query: 306 RDFLIQGLGELGWDVPKTKATMYLWVKCPVGMGST-DFALNLLQQTGVVVTPGNAFGVAG 364
           R    + +  LG    + +  M+LW K P       +    +L Q  V +TPG  FG  G
Sbjct: 308 RHLAGEIMKTLGCTYDENQVGMFLWGKIPASCKDVEELTEKVLHQARVFITPGFIFGSNG 367

Query: 365 EGYVRISLIADCDRLGEALDRIKQ 388
             ++RISL     +L EAL+RIK+
Sbjct: 368 ARFIRISLCCKDAKLAEALERIKK 391


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: 420
Number of extensions: 21
Number of successful extensions: 3
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: 393
Length adjustment: 31
Effective length of query: 372
Effective length of database: 362
Effective search space:   134664
Effective search space used:   134664
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 09 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