Align delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial; EC 1.5.1.12 (characterized)
to candidate PfGW456L13_1397 Aldehyde dehydrogenase (EC 1.2.1.3)
Query= CharProtDB::CH_122352 (572 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1397 Length = 496 Score = 162 bits (411), Expect = 2e-44 Identities = 145/472 (30%), Positives = 228/472 (48%), Gaps = 37/472 (7%) Query: 75 KEVKSSSSLTQSNPASHGPVATYSNATAKDVQAAIESALEARKS--WASTPFADRASVFL 132 + +S + NPA+ +A + +DV AA+ +A + ++ WA+ +R V L Sbjct: 27 RPAQSGQTFAAINPATSQCLANVAACGEEDVNAAVHNARQVFEAGTWAARSPTERKQVLL 86 Query: 133 KAADLISTKYRYDVMALTMHGQGK---NAWQAEIDSAAELCDFFRFGVKYAEDLYAQQPV 189 + ADLI + R ++ L GK +A+ ++ AA + FR+ + + LY Q Sbjct: 87 RLADLI-LENREELALLDSLNMGKPVADAYNIDVPGAAGV---FRWYAESLDKLYDQV-- 140 Query: 190 HHAPGVWNRVEY--RPLEGFVYAISPFNFTAIGGNLAGAPALM-GNVVVWKPSPSAIASN 246 AP N + R G V A+ P+NF APAL GN V+ KP+ + S Sbjct: 141 --APSAQNVLATITREALGVVAAVVPWNFPLDMAAWKLAPALAAGNSVILKPAEQSPFSA 198 Query: 247 WLVHQILLEAGLPKNVIQFVPGEAEEVTKTVLDHPDFAALHFTGSTNVFRNLYGQISTRV 306 + ++ LEAG+P V+ +PG E+ K + HPD L FTGST V + + Q S + Sbjct: 199 LRLAELALEAGVPAGVLNVLPGLGEQTGKALGLHPDVDCLVFTGSTEVGK-YFMQYSAQ- 256 Query: 307 AAGKYRSYPRIVGETGGKNFHLIHKSA-DIRNAAVQTVRGAFEYQGQKCSATSRVYVASS 365 + ++ E GGK+ +L+ D+ AA + G F QG+ CSA SR+ V S Sbjct: 257 -----SNLKQVWLECGGKSANLVFADCQDLDLAAEKAAFGIFFNQGEVCSANSRLLVQRS 311 Query: 366 IADSFLEQVASEAKSLKVGPPSDFTNFCGPVIHEASFTKLAKVIDEAKNDPELELLAG-G 424 I D F+E++ ++A+ G P D ++ G ++ ++ K I +A+ + G Sbjct: 312 IHDEFVERLKAQAERWLPGDPLDPSSAAGAIVDSRQTARIMKFIQQAEQQGATRICGGRQ 371 Query: 425 SYDSSKGWYIQPTVYRTTNPDHPLLTRELFGPILVVYAYPDATEADFARIAQKIDATGEY 484 S + +IQPT++ PD PL E+FGP+L V A+ D EA ++A Y Sbjct: 372 SIINGSDNFIQPTIFTGVTPDMPLFRDEVFGPVLAVTAFDD--EAHALQLAN----DSVY 425 Query: 485 GLTGSVFAQDREALAVANDVLRN-AAGNFYINCKSTGAVVGQQPFGGARASG 535 GL S++ D L A+ V R AG +N S A+ PFGG + SG Sbjct: 426 GLAASLWTDD---LNRAHRVARQLRAGTVSVN--SVDALDVTVPFGGGKQSG 472 Lambda K H 0.316 0.130 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: 587 Number of extensions: 33 Number of successful extensions: 5 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: 572 Length of database: 496 Length adjustment: 35 Effective length of query: 537 Effective length of database: 461 Effective search space: 247557 Effective search space used: 247557 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 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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