GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Rhodospirillum rubrum ATCC 11170

Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate WP_011391014.1 RRU_RS16855 homoserine O-acetyltransferase

Query= curated2:A0LCI7
         (394 letters)



>NCBI__GCF_000013085.1:WP_011391014.1
          Length = 391

 Score =  390 bits (1002), Expect = e-113
 Identities = 197/358 (55%), Positives = 249/358 (69%), Gaps = 8/358 (2%)

Query: 26  PLQLDGGTLLHSVDVSYETYGTLNQERSNAVLICHALSGNAHAAGYHSKDDKRPGWWDHY 85
           P++LD G  L  + V+Y+T G LN ER+NA+LICHAL+G+ H  G H     RPGWW+  
Sbjct: 22  PMRLDSGLELGPLTVAYQTIGRLNAERTNAILICHALTGDQHVIGPHPVTG-RPGWWETL 80

Query: 86  IGPGKPFDTNRYFVIASNNLGGCDGTTGPSSIDPATGMPYGLNFPMITIGDIVRVQHALV 145
           +GPGK  DT+RYF+I SN LGGC GTTGP  I+PATG P+GL FP+ITIGD+VR Q  L+
Sbjct: 81  VGPGKTIDTDRYFIICSNVLGGCLGTTGPKEINPATGKPWGLGFPVITIGDMVRAQALLL 140

Query: 146 RQLGIERLMAVVGGSMGGMQALQWALDYPHMVPASVIIAAAPRLTAQNIAFNAVARQAIM 205
             LGIERL   +GGSMG MQ LQWA+ YP  V A V IA + R +AQNIAF+ V RQAIM
Sbjct: 141 DHLGIERLFCAIGGSMGAMQVLQWAVSYPERVRAVVPIAGSWRHSAQNIAFHEVGRQAIM 200

Query: 206 ADPHFNGGDYYTLPGDPTTKARPESGLALARMMAHITYLSEQGLHERFGRRLQDRDALSY 265
           ADP +NGGDY            P  GLA+ARM AHITYLSE  L  +FGR+LQDR +++Y
Sbjct: 201 ADPDWNGGDYL------NQGTVPRRGLAVARMTAHITYLSEPALQSKFGRKLQDRASITY 254

Query: 266 GFETDFAVESYLSYQGSSFVKRFDANSYLYITKAMDYFDPFPDAETTVQR-LTGVESHFL 324
           GF+ DF VESYL +QG++FVKRFDANSYLYIT+AMDYFD   + +  + R   G +  F 
Sbjct: 255 GFDADFQVESYLRHQGANFVKRFDANSYLYITRAMDYFDLAAEHDGVLARAFQGTKVRFC 314

Query: 325 VMSFDTDWRFDTSRSKELVRILHRSLKDCTFQEFSSPAGHDAFLLPHPSYEKSLGSFL 382
           V+SF +DW F T+ S+ +VR ++ +  D +F E ++  GHDAFLL  P +  +L  FL
Sbjct: 315 VVSFTSDWLFPTAESRAVVRAMNAAAADVSFVEVTTDKGHDAFLLDEPEFHDTLQGFL 372


Lambda     K      H
   0.320    0.136    0.417 

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: 508
Number of extensions: 28
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: 394
Length of database: 391
Length adjustment: 31
Effective length of query: 363
Effective length of database: 360
Effective search space:   130680
Effective search space used:   130680
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 Jul 25 2024. The underlying query database was built on Jul 25 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