GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_3 in Mesorhizobium ciceri WSM1271

Align Methionine synthase component, pterin-binding domain (EC:2.1.1.13) (characterized)
to candidate YP_004142536.1 Mesci_3363 methionine synthase

Query= reanno::Phaeo:GFF1582
         (353 letters)



>NCBI__GCF_000185905.1:YP_004142536.1
          Length = 324

 Score =  395 bits (1015), Expect = e-115
 Identities = 217/367 (59%), Positives = 257/367 (70%), Gaps = 62/367 (16%)

Query: 1   MTRTVVESKTKTAILGFDEPFCVIGERINPTGRKKLAAELEAGDFSTVEKDALAQVMAGA 60
           MTRT+V S T+  I+GFD+PFCVIGERINPTGRKKLAAE+ AG+F TV +DAL Q   GA
Sbjct: 1   MTRTIVASATREIIIGFDQPFCVIGERINPTGRKKLAAEMIAGNFETVIRDALEQAACGA 60

Query: 61  NILDINAGVVYNSNPNPNETEPPLMTKIVELVQGLTDTPLCIDSSVPGALEAGLQAAEGR 120
            +LD+NAGV   ++ NPNETEP L+ + +E+VQGL D PL IDSSV  A+EA L+ A+GR
Sbjct: 61  TMLDVNAGV---TSVNPNETEPGLLVQTLEIVQGLVDLPLSIDSSVTAAIEAALKVAKGR 117

Query: 121 PLLNSVTGEEERLEHVLPLVKKYNVPVVAISNDDTGISEDPDVRFAVAKKIVERAADFGI 180
           PL+NSVTGEEE+LE +LPLVKKYNVPVVAISND+TGIS DPDVRFAVAKKIVER ADFGI
Sbjct: 118 PLVNSVTGEEEKLEAILPLVKKYNVPVVAISNDETGISMDPDVRFAVAKKIVERCADFGI 177

Query: 181 PAHDIVVDPLVMPIGAMATAGQQVFALVRRLREELGVNTTCGASNVSFGLPNRHGINNAF 240
           PAHD+VVDPLVMPIGA+  AG+QVFAL+RRLREEL VNTTCG SN+SFGLP+RHGIN AF
Sbjct: 178 PAHDVVVDPLVMPIGALGDAGRQVFALLRRLREELKVNTTCGLSNISFGLPHRHGINAAF 237

Query: 241 LPMAMGAGMTSAIMNPVALPITQKKIAEKKAEVEAAGIILPEGMEDEAFVQMFGLGSTKP 300
           +PM +GAGMTSAIMNPV                                         +P
Sbjct: 238 IPMVIGAGMTSAIMNPV-----------------------------------------RP 256

Query: 301 RAGKEMEAIRAANLLTNNDPHGGEWIKANKE--PAKEGE------------EGRGRGG-R 345
              +EMEA+R AN+L   D +   WI+  K+  PA+ G+            +G G GG R
Sbjct: 257 ---QEMEAVRGANVLNGTDENCTNWIRTYKDYKPAEGGQAVAAPTQVNAPGDGAGNGGRR 313

Query: 346 AGGRRRR 352
            GGR  R
Sbjct: 314 RGGREAR 320


Lambda     K      H
   0.315    0.134    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: 368
Number of extensions: 10
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 353
Length of database: 324
Length adjustment: 28
Effective length of query: 325
Effective length of database: 296
Effective search space:    96200
Effective search space used:    96200
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: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 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