GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Marinobacter adhaerens HP15

Align alanine—glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate GFF835 HP15_814 aspartate aminotransferase

Query= metacyc::MONOMER-21143
         (387 letters)



>FitnessBrowser__Marino:GFF835
          Length = 416

 Score =  216 bits (551), Expect = 7e-61
 Identities = 114/358 (31%), Positives = 193/358 (53%), Gaps = 2/358 (0%)

Query: 25  LEAQGKPMIHLGLGQPDFKTPQHVVDAAKKALDEGHHGYVLSNGILECRQAVTRKIKKLY 84
           + A  K +IHL +GQPD  TP+HV+DA   AL+ G  GY +  G+ E   A+     K Y
Sbjct: 52  MAATMKDVIHLSIGQPDLPTPKHVIDAYIDALNAGQTGYTMDAGLPELLVALRDYYGKRY 111

Query: 85  NKDIDPERVLIMPGGKPTMYYAIQCFGEPGAEIIHPTPAFPIYESMINYTGSTPVPYDLT 144
           N+ +  + +LI  G    MY AI     PG + I   P+F +Y  +I   G         
Sbjct: 112 NRKLTRDNILITSGATEAMYLAISATSAPGRQFIVTDPSFLLYAPLIRMNGGEVKFVQTR 171

Query: 145 EDKDLKFDPEKILSLITDKTRLLILINPNNPTGSFVEKSAIDVLAEGLKKHPHVAILSDE 204
            + + + DP++++  +  +T  LIL NPNNPTG+   +S ++ + E    +  + + +DE
Sbjct: 172 AENNHQLDPDEVIKAMGPRTYALILNNPNNPTGAVYPRSTVETILEEC-AYRGIQVYADE 230

Query: 205 IYSRQIYDGKEMPTFFNYPDLQDRLIVLDGWSKAYAMTGWRMGWSVWPEELIPHVNKLII 264
           +Y   I+D ++  +  N     D ++ +  +SK Y+M G R+GW +  +  I  + +  +
Sbjct: 231 VYDHLIFDDEDFASVLNCSMDLDNIMCISSFSKTYSMAGLRVGWVIASQAAIKSLRRFHM 290

Query: 265 NSVSCVNAPSQFAGIAALDGPDDAIHEMMVKFDQRRKLIHEGLNSLPGVECSLPGGAFYA 324
            + S  N PSQFAG+AAL G    + +M+  + +RR  + E ++  P +    PGGAF+A
Sbjct: 291 FTTSVANTPSQFAGVAALTGDQQCVRDMVDIYRERRDKVVELVDQTPYMTGYKPGGAFFA 350

Query: 325 FPKVIGTGMNGSEFAKKCMHEAGVAIVPGTAFGKTCQDYVRFSYAASQDNISNALENI 382
           FP  +   ++GS+ A + + E GV +VPG AFG+ C + VR S++ + + +  A + +
Sbjct: 351 FPD-LPPHVDGSDLALRMLKETGVCMVPGDAFGEGCTNAVRISFSTTCEKLEEAFDRV 407


Lambda     K      H
   0.319    0.137    0.414 

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: 444
Number of extensions: 17
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: 387
Length of database: 416
Length adjustment: 31
Effective length of query: 356
Effective length of database: 385
Effective search space:   137060
Effective search space used:   137060
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 (21.7 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