GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pseudomonas putida KT2440

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate PP_0858 PP_0858 putative methionine/glutamine aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Putida:PP_0858
          Length = 382

 Score =  177 bits (448), Expect = 6e-49
 Identities = 119/358 (33%), Positives = 181/358 (50%), Gaps = 16/358 (4%)

Query: 36  LTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPELREALAEKFRRENGLSV-TPEET 94
           L+ G PDF+ P+ + +A  R +A G  +Y+P  G+P LR+ +A K  R  G  V   +E 
Sbjct: 29  LSQGFPDFNGPQALLDAVGRHVAAGHNQYSPMTGLPALRQQVAAKVERLYGARVDADQEV 88

Query: 95  IVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGVVVEVETLPEEGFVPDP 154
            +T G  +A+F   QA++  GDEVIV  P + SY   V  AGG  V V+ L +  F  D 
Sbjct: 89  TITPGATEAIFCAIQAVVHAGDEVIVFDPCYDSYEPSVELAGGRCVHVQ-LSDGDFRIDW 147

Query: 155 ERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVEHDFYLVSDEIYEHLLYEGE 214
           ++   A++PRT+ +++NSP+NP+GA+  +E L+ LA L  + D YLVSDE+YEHL+Y+G 
Sbjct: 148 QKFSDALSPRTRMVILNSPHNPSGALITREDLDQLAALIADRDIYLVSDEVYEHLVYDGV 207

Query: 215 HFSPGRVAPE---HTLTVNGAAKAFAMTGWRIGYACGPKEVIKAMASVSSQSTTSPDTIA 271
             +      +       V+   K + +TGW+ GY   P  +   +  V         T  
Sbjct: 208 RHASVLAHEQLYSRAFVVSSFGKTYHVTGWKTGYVIAPPALSAELRKVHQYVNFCGVTPL 267

Query: 272 QWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTALGLKAVRPSGAFYVLMDTSPIA 331
           Q A  + +         ++     Y+ +RDL    L        R +G ++ L+D S I 
Sbjct: 268 QCALADFMAGHP---EHIDELPAFYQAKRDLFCGLLDGSRFNFTRTTGTYFQLVDYSQIR 324

Query: 332 PD--EVRAAERLL-EAGVAVVPGTDF-----AAFGHVRLSYATSEENLRKALERFARV 381
           PD  +V  +  L  E GVA +P + F          VRL +A  EE LR+A ER   +
Sbjct: 325 PDLNDVDMSLWLTREHGVATIPVSVFYQQPIPEQRLVRLCFAKREETLRQAAERLCAI 382


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: 328
Number of extensions: 20
Number of successful extensions: 5
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: 382
Length adjustment: 30
Effective length of query: 355
Effective length of database: 352
Effective search space:   124960
Effective search space used:   124960
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