Align Formate-dependent phosphoribosylglycinamide formyltransferase; 5'-phosphoribosylglycinamide transformylase 2; Formate-dependent GAR transformylase; GAR transformylase 2; GART 2; Non-folate glycinamide ribonucleotide transformylase; Phosphoribosylglycinamide formyltransferase 2; EC 2.1.2.- (characterized)
to candidate Synpcc7942_0588 Synpcc7942_0588 phosphoribosylglycinamide formyltransferase 2
Query= SwissProt::P33221 (392 letters) >FitnessBrowser__SynE:Synpcc7942_0588 Length = 391 Score = 387 bits (993), Expect = e-112 Identities = 213/380 (56%), Positives = 263/380 (69%), Gaps = 2/380 (0%) Query: 14 RVMLLGSGELGKEVAIECQRLGVEVIAVDRYADAPAMHVAHRSHVINMLDGDALRRVVEL 73 R+MLLGSGELGKE AI QRLG VIAVDRYA APAM VA S VI+MLDG+AL VV+ Sbjct: 10 RLMLLGSGELGKEFAIAAQRLGNTVIAVDRYAHAPAMQVADASAVISMLDGEALEAVVQE 69 Query: 74 EKPHYIVPEIEAIATDMLIQLEEEGLNVVPCARATKLTMNREGIRRLAAEELQLPTSTYR 133 +P I+PEIEAI T+ L + E+ GL V+P ARAT TMNR+ IR LAA++L L T+ Y Sbjct: 70 FQPDLIIPEIEAIRTEKLQEFEDRGLTVIPTARATHFTMNRDRIRDLAAQQLGLRTARYA 129 Query: 134 FADSESLFREAVADIGYPCIVKPVMSSSGKGQTFIRSAEQLAQAWKYAQQGGRAGAGRVI 193 +A + A IGYP ++KPVMSSSGKGQ+ I+ +QL AW YA G R + +VI Sbjct: 130 YASCFEELQTVAAAIGYPNVIKPVMSSSGKGQSIIQQPDQLQAAWDYAIAGSRGDSQKVI 189 Query: 194 VEGVVKFDFEITLLTVSAVDG-VHFCAPVGHRQEDGDYRESWQPQQMSPLALERAQEIAR 252 +E + F+ EITLLT+ G FC P+GHRQE GDY+ESWQP + P L +AQ IA Sbjct: 190 LEEFIPFELEITLLTIRQWQGPTLFCPPIGHRQERGDYQESWQPAPLRPDLLAQAQAIAA 249 Query: 253 KVVLALGGYGLFGVELFVCGDEVIFSEVSPRPHDTGMVTLISQDLSEFALHVRAFLGLPV 312 +V ALGG GLFGVE FV DEVIFSE+SPRPHDTGMVTLISQ+L+EF LH+RA LGLP+ Sbjct: 250 QVTEALGGAGLFGVEFFVTPDEVIFSELSPRPHDTGMVTLISQNLNEFELHLRAVLGLPI 309 Query: 313 GGIRQYGPAASAVILPQLTSQNVTFDNVQNAVGAD-LQIRLFGKPEIDGSRRLGVALATA 371 I GP+AS VIL + + ++ V A+ + +RLFGKP++ RR+GVALA Sbjct: 310 PAIELLGPSASRVILAEDSGDRPSYAGVAAALQEPWVDLRLFGKPDMRPQRRMGVALARD 369 Query: 372 ESVVDAIERAKHAAGQVKVQ 391 ESV A +A AA QV +Q Sbjct: 370 ESVEAARAKADRAASQVTIQ 389 Lambda K H 0.320 0.136 0.390 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: 410 Number of extensions: 15 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: 392 Length of database: 391 Length adjustment: 31 Effective length of query: 361 Effective length of database: 360 Effective search space: 129960 Effective search space used: 129960 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 Apr 09 2024. The underlying query database was built on Sep 17 2021.
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:
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