GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Marinobacter adhaerens HP15

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate GFF835 HP15_814 aspartate aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Marino:GFF835
          Length = 416

 Score =  193 bits (490), Expect = 8e-54
 Identities = 114/353 (32%), Positives = 192/353 (54%), Gaps = 11/353 (3%)

Query: 32  DLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPELREALAEKFRRENGLSVTP 91
           D++ L+ G+PD  TP+HV +A   AL  G+T Y   AG+PEL  AL + + +     +T 
Sbjct: 58  DVIHLSIGQPDLPTPKHVIDAYIDALNAGQTGYTMDAGLPELLVALRDYYGKRYNRKLTR 117

Query: 92  EETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGVVVEVETLPEEGFV 151
           +  ++T G  +A++    A   PG + IV  P ++ Y  ++R  GG V  V+T  E    
Sbjct: 118 DNILITSGATEAMYLAISATSAPGRQFIVTDPSFLLYAPLIRMNGGEVKFVQTRAENNHQ 177

Query: 152 PDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVEHDFYLVSDEIYEHLLY 211
            DP+ V +A+ PRT AL++N+PNNPTGAVYP+  +E +          + +DE+Y+HL++
Sbjct: 178 LDPDEVIKAMGPRTYALILNNPNNPTGAVYPRSTVETILEECAYRGIQVYADEVYDHLIF 237

Query: 212 EGEHFSP---GRVAPEHTLTVNGAAKAFAMTGWRIGYACGPKEVIKAMASVSSQSTTSPD 268
           + E F+      +  ++ + ++  +K ++M G R+G+    +  IK++      +T+  +
Sbjct: 238 DDEDFASVLNCSMDLDNIMCISSFSKTYSMAGLRVGWVIASQAAIKSLRRFHMFTTSVAN 297

Query: 269 TIAQWATLEALT-NQEASRAFVEMAREAYRRRRDLLLEGLTALG-LKAVRPSGAFYVLMD 326
           T +Q+A + ALT +Q+  R  V++    YR RRD ++E +     +   +P GAF+   D
Sbjct: 298 TPSQFAGVAALTGDQQCVRDMVDI----YRERRDKVVELVDQTPYMTGYKPGGAFFAFPD 353

Query: 327 TSPIAPDEVRAAERLLEAGVAVVPGTDF--AAFGHVRLSYATSEENLRKALER 377
             P       A   L E GV +VPG  F       VR+S++T+ E L +A +R
Sbjct: 354 LPPHVDGSDLALRMLKETGVCMVPGDAFGEGCTNAVRISFSTTCEKLEEAFDR 406


Lambda     K      H
   0.317    0.133    0.379 

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: 367
Number of extensions: 19
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: 385
Length of database: 416
Length adjustment: 31
Effective length of query: 354
Effective length of database: 385
Effective search space:   136290
Effective search space used:   136290
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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