Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4IB59
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006979 | response to oxidative stress | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016485 | protein processing | 5 | 1 |
GO:0016540 | protein autoprocessing | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008234 | cysteine-type peptidase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 215 | 221 | PF00089 | 0.346 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.509 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.269 |
DOC_CYCLIN_yCln2_LP_2 | 208 | 214 | PF00134 | 0.304 |
DOC_CYCLIN_yCln2_LP_2 | 312 | 318 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 294 | 301 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 61 | 69 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.314 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.304 |
DOC_PP2B_LxvP_1 | 414 | 417 | PF13499 | 0.652 |
DOC_PP2B_LxvP_1 | 421 | 424 | PF13499 | 0.567 |
DOC_PP4_MxPP_1 | 348 | 351 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.307 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 339 | 344 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.522 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_Clathr_ClatBox_1 | 165 | 169 | PF01394 | 0.356 |
LIG_Clathr_ClatBox_1 | 24 | 28 | PF01394 | 0.413 |
LIG_eIF4E_1 | 313 | 319 | PF01652 | 0.436 |
LIG_EVH1_1 | 366 | 370 | PF00568 | 0.459 |
LIG_EVH1_1 | 414 | 418 | PF00568 | 0.711 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.421 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.301 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.734 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.281 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.388 |
LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 281 | 287 | PF02991 | 0.216 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 441 | 445 | PF02991 | 0.719 |
LIG_NRBOX | 282 | 288 | PF00104 | 0.402 |
LIG_Pex14_1 | 382 | 386 | PF04695 | 0.718 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.736 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.456 |
LIG_SH2_GRB2like | 282 | 285 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 422 | 426 | PF00017 | 0.601 |
LIG_SH2_PTP2 | 214 | 217 | PF00017 | 0.421 |
LIG_SH2_SRC | 282 | 285 | PF00017 | 0.356 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.623 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.321 |
LIG_SH2_STAT3 | 227 | 230 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.732 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.319 |
LIG_SH3_1 | 374 | 380 | PF00018 | 0.714 |
LIG_SH3_1 | 386 | 392 | PF00018 | 0.706 |
LIG_SH3_2 | 47 | 52 | PF14604 | 0.449 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.370 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.359 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.440 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.668 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.647 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.668 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.607 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.658 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.636 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.708 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.401 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 3 | 9 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 23 | 28 | PF11976 | 0.412 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.421 |
LIG_UBA3_1 | 165 | 172 | PF00899 | 0.419 |
LIG_WRPW_2 | 313 | 316 | PF00400 | 0.462 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.353 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.388 |
MOD_Cter_Amidation | 37 | 40 | PF01082 | 0.508 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.272 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.426 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.185 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.275 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.267 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.349 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.303 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.275 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.385 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.650 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.363 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.388 |
MOD_LATS_1 | 170 | 176 | PF00433 | 0.419 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.421 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.296 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.445 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.344 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.253 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.334 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.288 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.273 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.657 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.491 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.290 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.715 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.419 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.384 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.269 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.417 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.411 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.560 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.385 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.270 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.454 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.415 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.696 |
TRG_DiLeu_BaEn_1 | 101 | 106 | PF01217 | 0.281 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.512 |
TRG_NLS_MonoExtC_3 | 293 | 298 | PF00514 | 0.421 |
TRG_NLS_MonoExtN_4 | 294 | 299 | PF00514 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW49 | Leptomonas seymouri | 49% | 98% |
A0A0N1P9F5 | Leptomonas seymouri | 44% | 100% |
A0A0N1PDW0 | Leptomonas seymouri | 74% | 100% |
A0A0S4IS06 | Bodo saltans | 44% | 100% |
A0A0S4J2H4 | Bodo saltans | 53% | 98% |
A0A1X0NMB0 | Trypanosomatidae | 48% | 100% |
A0A1X0NMU0 | Trypanosomatidae | 49% | 100% |
A0A1X0P5R0 | Trypanosomatidae | 57% | 100% |
A0A3Q8IG58 | Leishmania donovani | 98% | 100% |
A0A422N5J3 | Trypanosoma rangeli | 48% | 100% |
A0A422NQE5 | Trypanosoma rangeli | 65% | 97% |
A1CL82 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 37% | 100% |
A1D611 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 37% | 100% |
A2QU58 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 38% | 100% |
A4HMH9 | Leishmania braziliensis | 82% | 97% |
A5DZS4 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 37% | 100% |
A6SDT7 | Botryotinia fuckeliana (strain B05.10) | 37% | 100% |
A6ZP43 | Saccharomyces cerevisiae (strain YJM789) | 37% | 100% |
A7F075 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 38% | 100% |
B0Y081 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 37% | 100% |
C9ZQB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZQB1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZZG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 91% |
D0A1S2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AEY0 | Leishmania major | 94% | 97% |
E9B636 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
P0CM58 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 36% | 97% |
P0CM59 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 36% | 97% |
Q08601 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 100% |
Q0CQL9 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 37% | 100% |
Q2UCB7 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 37% | 100% |
Q2VLK6 | Trypanosoma cruzi (strain CL Brener) | 46% | 100% |
Q2VLK8 | Trypanosoma cruzi (strain CL Brener) | 64% | 100% |
Q4WYT0 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 37% | 100% |
Q585F3 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 49% | 100% |
Q5ANA8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 37% | 100% |
Q6CLS0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 38% | 100% |
Q75B43 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 35% | 99% |
Q7S4N5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 37% | 100% |
Q7XJE6 | Arabidopsis thaliana | 31% | 100% |
Q8IEW1 | Trypanosoma brucei brucei | 56% | 90% |
Q8T8E5 | Trypanosoma brucei brucei | 40% | 100% |
Q8T8E6 | Trypanosoma brucei brucei | 48% | 100% |
Q8T8E7 | Trypanosoma brucei brucei | 49% | 100% |
V5BTK1 | Trypanosoma cruzi | 63% | 100% |