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 WP_019557476.1 F612_RS0109205 formate-dependent phosphoribosylglycinamide formyltransferase
Query= SwissProt::P33221 (392 letters) >NCBI__GCF_000381085.1:WP_019557476.1 Length = 396 Score = 504 bits (1298), Expect = e-147 Identities = 256/394 (64%), Positives = 307/394 (77%), Gaps = 4/394 (1%) Query: 1 MTLLGTALRPAATRVMLLGSGELGKEVAIECQRLGVEVIAVDRYADAPAMHVAHRSHVIN 60 M+ +GT A RV+L G+GELGKEVAIE QRLGVEVIA DRYA+APAM VA RSHV++ Sbjct: 1 MSNIGTPFSSTAVRVLLCGAGELGKEVAIELQRLGVEVIAADRYANAPAMQVADRSHVVD 60 Query: 61 MLDGDALRRVVELEKPHYIVPEIEAIATDMLIQLEEEGLNVVPCARATKLTMNREGIRRL 120 MLDG ALR+V+ELEKPH +VPEIEAIATD L +LE EG+ ++P ARAT+LTMNREGIRRL Sbjct: 61 MLDGAALRKVIELEKPHMVVPEIEAIATDTLAELENEGVKIIPTARATQLTMNREGIRRL 120 Query: 121 AAEELQLPTSTYRFADSESLFREAVADIGYPCIVKPVMSSSGKGQTFIRSAEQLAQAWKY 180 AAE L +PTS Y F D+++ F A+ IG PC+VKP+MSSSGKGQ+ I++A + QAW Y Sbjct: 121 AAEALGIPTSPYEFVDTKADFEAAIGRIGMPCVVKPIMSSSGKGQSVIKTAADINQAWSY 180 Query: 181 AQQGGRAGAGRVIVEGVVKFDFEITLLTVSAVDGVHFCAPVGHRQEDGDYRESWQPQQMS 240 AQ+GGRAG GRVI+EG V+FD+EITLLTV G+ FC P+GH QEDGDYR+SWQPQ MS Sbjct: 181 AQEGGRAGKGRVIIEGFVEFDYEITLLTVRHEQGISFCEPIGHHQEDGDYRQSWQPQVMS 240 Query: 241 PLALERAQEIARKVVLAL---GGYGLFGVELFVCGDEVIFSEVSPRPHDTGMVTLISQDL 297 A+ +QEIARKV L G GLFGVELF+ GD V FSEVSPRPHDTG+VTL+SQDL Sbjct: 241 AAAITTSQEIARKVTDNLCGETGRGLFGVELFIKGDNVYFSEVSPRPHDTGLVTLMSQDL 300 Query: 298 SEFALHVRAFLGLPVGGIRQYGPAASAVILPQLTSQNVTFDNVQNAVG-ADLQIRLFGKP 356 SEFALH RA LGLP+ IRQ+GP AS+VILP S+ F N+ A+ D QIRLFGKP Sbjct: 301 SEFALHARAILGLPIPNIRQHGPTASSVILPTGKSRQTEFSNLTEALSLPDTQIRLFGKP 360 Query: 357 EIDGSRRLGVALATAESVVDAIERAKHAAGQVKV 390 EIDG RR+GVA+A A+++ +AI +A A VKV Sbjct: 361 EIDGRRRMGVAIAKADTIEEAINKANQVAAAVKV 394 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: 451 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: 392 Length of database: 396 Length adjustment: 31 Effective length of query: 361 Effective length of database: 365 Effective search space: 131765 Effective search space used: 131765 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