GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pseudomonas fluorescens FW300-N2C3

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate AO356_22880 AO356_22880 aspartate aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_22880
          Length = 395

 Score =  255 bits (652), Expect = 1e-72
 Identities = 148/365 (40%), Positives = 210/365 (57%), Gaps = 9/365 (2%)

Query: 19  VNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPELREALA 78
           ++ +AL +R QG+D++ L+ G+PDFDTP  + +AA  +L  G T Y+   G+  LR ++A
Sbjct: 20  IHDRALAMREQGMDVLLLSVGDPDFDTPRAIVDAAVGSLRAGDTHYSDIRGLHTLRSSIA 79

Query: 79  EKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGV 138
            + R   GL V  E  +V  G + A++ + Q +L+ GDEVIV  P +V+Y  +    G  
Sbjct: 80  RRHRLRCGLGVGAEHVVVLPGAQCAVYAVAQCLLNAGDEVIVAEPMYVTYEAVFGACGAK 139

Query: 139 VVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVEHDF 198
           VV V   PE GF  +P  V R ITPRT+A+++NSPNNP+GA  P    +ALARL +EHD 
Sbjct: 140 VVPVAVRPENGFRVEPADVARLITPRTRAMLLNSPNNPSGASLPMSTWQALARLCIEHDL 199

Query: 199 YLVSDEIYEHLLYEGEHFSPGRV--APEHTLTVNGAAKAFAMTGWRIGYACGPKEVIKAM 256
           +L+SDE+Y  L+YEGEH SP  +    E T T+N  +K+ AMTGWRIG+  GP+ +   +
Sbjct: 200 WLISDEVYSDLIYEGEHISPASLPGMAERTATINSLSKSHAMTGWRIGWVIGPQALAGHL 259

Query: 257 ASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGL-TALGLKAV 315
           A++S           Q A   AL   E +   V    E YR+RRDL+   L    GLK V
Sbjct: 260 ANLSLCMLFGLPDFVQRAAQVAL---EQALPEVAQMHEEYRQRRDLVCAMLDDCPGLKPV 316

Query: 316 RPSGAFYVLMDTSPIAPDEVRAAERLLEA-GVAVVPGTDF--AAFGHVRLSYATSEENLR 372
           RP G  +V++D      D    AERLL+  GV+V+ G  F  +A GH+R+     +  L 
Sbjct: 317 RPDGGMFVMVDVRQTGLDAQVFAERLLDGYGVSVLAGEAFGPSAAGHIRIGLVVDQVKLA 376

Query: 373 KALER 377
            A  R
Sbjct: 377 DACRR 381


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: 384
Number of extensions: 10
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: 385
Length of database: 395
Length adjustment: 31
Effective length of query: 354
Effective length of database: 364
Effective search space:   128856
Effective search space used:   128856
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