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 |
Related structures:
AlphaFold database: A0A3Q8ICU5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.554 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.598 |
DOC_MAPK_gen_1 | 288 | 296 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 158 | 165 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 384 | 391 | PF00149 | 0.496 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.694 |
DOC_USP7_UBL2_3 | 395 | 399 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 136 | 146 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 291 | 295 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 353 | 358 | PF00244 | 0.466 |
LIG_BIR_III_4 | 153 | 157 | PF00653 | 0.657 |
LIG_Dynein_DLC8_1 | 458 | 464 | PF01221 | 0.503 |
LIG_eIF4E_1 | 215 | 221 | PF01652 | 0.542 |
LIG_EVH1_1 | 243 | 247 | PF00568 | 0.620 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.382 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.510 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.539 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.491 |
LIG_GBD_Chelix_1 | 321 | 329 | PF00786 | 0.527 |
LIG_LIR_Gen_1 | 111 | 118 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 159 | 168 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.477 |
LIG_LIR_LC3C_4 | 293 | 296 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.486 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.588 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.436 |
LIG_PCNA_PIPBox_1 | 55 | 64 | PF02747 | 0.515 |
LIG_PCNA_yPIPBox_3 | 53 | 62 | PF02747 | 0.503 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.360 |
LIG_Pex14_2 | 367 | 371 | PF04695 | 0.397 |
LIG_REV1ctd_RIR_1 | 389 | 399 | PF16727 | 0.529 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.404 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.527 |
LIG_SH3_1 | 439 | 445 | PF00018 | 0.582 |
LIG_SH3_2 | 442 | 447 | PF14604 | 0.636 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.699 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.582 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 217 | 222 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 337 | 343 | PF11976 | 0.367 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.502 |
MOD_CDK_SPxK_1 | 81 | 87 | PF00069 | 0.654 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.533 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.734 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.641 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.562 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.612 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.474 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.624 |
MOD_CMANNOS | 433 | 436 | PF00535 | 0.401 |
MOD_GlcNHglycan | 19 | 23 | PF01048 | 0.768 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.497 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.543 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.594 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.658 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.554 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.764 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.630 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.565 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.610 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.416 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.743 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.528 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.530 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.470 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.361 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.577 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.484 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.612 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.666 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.618 |
MOD_LATS_1 | 214 | 220 | PF00433 | 0.372 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.513 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.484 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.763 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.489 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.471 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.404 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.481 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.453 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.728 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.549 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.536 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.509 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.543 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.461 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.598 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.650 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.480 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.446 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.522 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.451 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.389 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.519 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.526 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.383 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.332 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.383 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.576 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.617 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.608 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.741 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.694 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.565 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.654 |
MOD_SUMO_for_1 | 5 | 8 | PF00179 | 0.792 |
MOD_SUMO_rev_2 | 375 | 380 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 51 | 61 | PF00179 | 0.589 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.525 |
TRG_NLS_MonoCore_2 | 11 | 16 | PF00514 | 0.715 |
TRG_NLS_MonoExtC_3 | 11 | 17 | PF00514 | 0.783 |
TRG_NLS_MonoExtN_4 | 9 | 16 | PF00514 | 0.735 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYW2 | Leptomonas seymouri | 57% | 100% |
A0A0S4IXA1 | Bodo saltans | 35% | 100% |
A0A1X0NVG3 | Trypanosomatidae | 30% | 91% |
A0A3R7KEJ9 | Trypanosoma rangeli | 44% | 100% |
A4HDE8 | Leishmania braziliensis | 76% | 100% |
A4I0T1 | Leishmania infantum | 100% | 100% |
D0A760 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AWT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QAP1 | Leishmania major | 92% | 100% |
V5BVT1 | Trypanosoma cruzi | 43% | 100% |