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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJY6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.365 |
DOC_CDC14_PxL_1 | 224 | 232 | PF14671 | 0.673 |
DOC_CYCLIN_yCln2_LP_2 | 368 | 371 | PF00134 | 0.517 |
DOC_MAPK_gen_1 | 108 | 114 | PF00069 | 0.658 |
DOC_MAPK_gen_1 | 128 | 134 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 135 | 143 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 256 | 264 | PF00069 | 0.662 |
DOC_MAPK_MEF2A_6 | 324 | 332 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 349 | 358 | PF00069 | 0.440 |
DOC_PP2B_LxvP_1 | 368 | 371 | PF13499 | 0.517 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.621 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.661 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 231 | 235 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 292 | 297 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 363 | 371 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 202 | 218 | PF00022 | 0.560 |
LIG_Actin_WH2_2 | 325 | 341 | PF00022 | 0.570 |
LIG_EH1_1 | 32 | 40 | PF00400 | 0.470 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.491 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.598 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.666 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.552 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.482 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.527 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.401 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.642 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.532 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.509 |
LIG_LIR_Apic_2 | 259 | 263 | PF02991 | 0.690 |
LIG_LIR_Gen_1 | 167 | 177 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 42 | 48 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.676 |
LIG_MYND_1 | 5 | 9 | PF01753 | 0.628 |
LIG_Pex14_2 | 121 | 125 | PF04695 | 0.300 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.582 |
LIG_SH2_NCK_1 | 333 | 337 | PF00017 | 0.605 |
LIG_SH2_PTP2 | 261 | 264 | PF00017 | 0.690 |
LIG_SH2_SRC | 261 | 264 | PF00017 | 0.690 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.341 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.468 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.532 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.632 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.707 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 162 | 169 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 355 | 360 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 87 | 93 | PF11976 | 0.636 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.343 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.357 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.585 |
LIG_TRFH_1 | 94 | 98 | PF08558 | 0.642 |
LIG_WRC_WIRS_1 | 20 | 25 | PF05994 | 0.701 |
LIG_WRC_WIRS_1 | 91 | 96 | PF05994 | 0.531 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.608 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.674 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.610 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.704 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.405 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.418 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.382 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.667 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.533 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.509 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.510 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.511 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.611 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.659 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.594 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.617 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.577 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.559 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.575 |
MOD_N-GLC_2 | 200 | 202 | PF02516 | 0.368 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.610 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.516 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.593 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.540 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.356 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.438 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.373 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.698 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.355 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.605 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.613 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.589 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.491 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.413 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.560 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.517 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.699 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.605 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.739 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.531 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.470 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.461 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.532 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.695 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.551 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.525 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.693 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.657 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.666 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.629 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.664 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.742 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.689 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.575 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.697 |
MOD_SUMO_rev_2 | 343 | 351 | PF00179 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.631 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P875 | Leptomonas seymouri | 62% | 100% |
A0A0S4JFY4 | Bodo saltans | 30% | 100% |
A0A1X0P6X1 | Trypanosomatidae | 33% | 87% |
A0A3R7M1V0 | Trypanosoma rangeli | 32% | 83% |
A0A3S7X519 | Leishmania donovani | 78% | 86% |
A4I7G9 | Leishmania infantum | 78% | 100% |
C9ZZZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 83% |
E9B2C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q5T0 | Leishmania major | 77% | 100% |
V5DTD7 | Trypanosoma cruzi | 31% | 82% |