Align δ1-pyrroline-5-carboxylate synthetase (EC 1.2.1.41; EC 2.7.2.11) (characterized)
to candidate H281DRAFT_06324 H281DRAFT_06324 glutamate-5-semialdehyde dehydrogenase
Query= metacyc::AT2G39800-MONOMER (717 letters) >FitnessBrowser__Burk376:H281DRAFT_06324 Length = 423 Score = 267 bits (682), Expect = 9e-76 Identities = 142/419 (33%), Positives = 235/419 (56%), Gaps = 14/419 (3%) Query: 292 DSNARDMAVAARESSRKLQALSSEDRKKILLDIADALEANVTTIKAENELDVASAQEAGL 351 D D+ AR++SR + S+ + L +A +E + +K N D+A A++ G Sbjct: 4 DQYMTDLGRRARQASRAMARASTAAKNAALAAVAAGIERDAALLKEANARDLARARDKGH 63 Query: 352 EESMVARLVMTPGKISSLAASVRKLADMEDPIGRVLKKTEVADGLVLEKTSSPLGVLLIV 411 + + + RL ++ + ++ +R++A + DPIG + G+ + + PLGV+ I+ Sbjct: 64 DAAFIDRLTLSDKALKTMVEGLRQVAALADPIGEISNLKYRPSGIQVGQMRVPLGVIGII 123 Query: 412 FESRPDALVQIASLAIRSGNGLLLKGGKEARRSNAILHKVITDAIPETVG----GKLIGL 467 +ESRP+ + A+L ++SGN +L+GG EA N L K+I + + E G + Sbjct: 124 YESRPNVTIDAAALCLKSGNATILRGGSEALECNTALAKLIGEGL-EAAGLPQDAVQVVA 182 Query: 468 VTSREEIPDLLKLDDVIDLVIPRGSNKLVTQIKNTTKIPVLGHADGICHVYVDKACDTDM 527 R + L+ + + +D+++PRG L+ ++ N ++P++ H DGICHVYVD D Sbjct: 183 TADRAAVGKLITMTEYVDVIVPRGGKSLIERLMNEARVPMIKHLDGICHVYVDDRADLAK 242 Query: 528 AKRIVSDAKLDYPAACNAMETLLVHKDLEQNAVL--------NELIFALQSNGVTLYGGP 579 A + +AK CN METLLV + + + E+ + + + G Sbjct: 243 ALTVCDNAKTHRYGTCNTMETLLVARGIASTVLPPLGKLYREKEVELRVDAAARAVLAGA 302 Query: 580 RASKILNIPEARSFNHEYCAKACTVEVVEDVYGAIDHIHRHGSAHTDCIVTEDHEVAELF 639 +++ E + EY A ++VV+D+ AI+HI+ + S HTD IVTEDH+ A F Sbjct: 303 GVGPLVDATED-DWRTEYLAPVLAIKVVDDLDAAIEHINTYSSQHTDAIVTEDHDRAMRF 361 Query: 640 LRQVDSAAVFHNASTRFSDGFRFGLGAEVGVSTGRIHARGPVGVEGLLTTRWIMRGKGQ 698 LR+VDSA+V NASTRF+DGF FGLGAE+G+S ++HARGPVG+EGL + ++++ G G+ Sbjct: 362 LREVDSASVMVNASTRFADGFEFGLGAEIGISNDKLHARGPVGLEGLTSLKYVVLGHGE 420 Lambda K H 0.318 0.135 0.378 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: 599 Number of extensions: 29 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: 717 Length of database: 423 Length adjustment: 36 Effective length of query: 681 Effective length of database: 387 Effective search space: 263547 Effective search space used: 263547 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: 53 (25.0 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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