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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9B6C9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.797 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.740 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.773 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.770 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.300 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.567 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.436 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.677 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 310 | 316 | PF00134 | 0.553 |
DOC_CYCLIN_yCln2_LP_2 | 42 | 45 | PF00134 | 0.698 |
DOC_MAPK_gen_1 | 500 | 510 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 99 | 107 | PF00069 | 0.612 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.668 |
DOC_PP4_FxxP_1 | 287 | 290 | PF00568 | 0.640 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.381 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 273 | 279 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 281 | 291 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 336 | 346 | PF00244 | 0.498 |
LIG_APCC_ABBA_1 | 36 | 41 | PF00400 | 0.511 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.649 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.565 |
LIG_CSL_BTD_1 | 226 | 229 | PF09270 | 0.592 |
LIG_deltaCOP1_diTrp_1 | 225 | 234 | PF00928 | 0.594 |
LIG_eIF4E_1 | 37 | 43 | PF01652 | 0.516 |
LIG_EVH1_1 | 43 | 47 | PF00568 | 0.589 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.626 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.547 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.648 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.609 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.583 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.483 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.582 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.634 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.672 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.689 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.522 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.515 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.565 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.588 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 269 | 274 | PF02991 | 0.550 |
LIG_LIR_Apic_2 | 285 | 290 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 159 | 167 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.518 |
LIG_MYND_1 | 40 | 44 | PF01753 | 0.537 |
LIG_PCNA_PIPBox_1 | 515 | 524 | PF02747 | 0.494 |
LIG_Pex14_1 | 478 | 482 | PF04695 | 0.409 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.482 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.519 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.556 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.701 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.696 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.569 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.523 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.603 |
LIG_SH3_5 | 327 | 331 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 506 | 513 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 103 | 109 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 506 | 513 | PF11976 | 0.536 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.648 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.399 |
LIG_WW_1 | 34 | 37 | PF00397 | 0.489 |
LIG_WW_2 | 51 | 54 | PF00397 | 0.672 |
MOD_CDK_SPxxK_3 | 205 | 212 | PF00069 | 0.473 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.589 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.608 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.585 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.714 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.571 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.421 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.648 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.774 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.606 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.636 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.600 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.706 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.647 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.589 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.650 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.567 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.591 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.585 |
MOD_Cter_Amidation | 441 | 444 | PF01082 | 0.645 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.527 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.685 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.676 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.551 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.589 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.582 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.701 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.708 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.718 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.600 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.689 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.634 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.742 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.516 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.539 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.536 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.645 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.508 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.715 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.585 |
MOD_PKA_1 | 212 | 218 | PF00069 | 0.670 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.602 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.577 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.590 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.519 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.715 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.520 |
MOD_Plk_2-3 | 450 | 456 | PF00069 | 0.671 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.507 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.466 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.598 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.486 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.764 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.627 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.609 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.578 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.651 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.621 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 547 | 550 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 184 | 191 | PF00179 | 0.627 |
TRG_DiLeu_BaEn_3 | 152 | 158 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 112 | 117 | PF01217 | 0.620 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.679 |
TRG_NLS_MonoExtC_3 | 211 | 216 | PF00514 | 0.733 |
TRG_NLS_MonoExtN_4 | 209 | 216 | PF00514 | 0.733 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEG0 | Leptomonas seymouri | 60% | 100% |
A0A1X0P5K7 | Trypanosomatidae | 34% | 100% |
A0A3Q8IJ29 | Leishmania donovani | 92% | 100% |
A0A3R7KY71 | Trypanosoma rangeli | 36% | 100% |
A4HMS3 | Leishmania braziliensis | 80% | 100% |
A4IBF9 | Leishmania infantum | 92% | 100% |
C9ZZA5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AF73 | Leishmania major | 90% | 100% |
V5DK90 | Trypanosoma cruzi | 35% | 100% |