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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B2Q7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.525 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.814 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.610 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.620 |
CLV_Separin_Metazoa | 242 | 246 | PF03568 | 0.618 |
DEG_APCC_DBOX_1 | 337 | 345 | PF00400 | 0.571 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.671 |
DEG_SCF_FBW7_1 | 173 | 180 | PF00400 | 0.567 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.726 |
DOC_CDC14_PxL_1 | 369 | 377 | PF14671 | 0.538 |
DOC_CYCLIN_RxL_1 | 233 | 246 | PF00134 | 0.628 |
DOC_CYCLIN_RxL_1 | 66 | 78 | PF00134 | 0.611 |
DOC_MAPK_gen_1 | 334 | 343 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.735 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.679 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.644 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 309 | 314 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 416 | 424 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 456 | 464 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 58 | 62 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.521 |
LIG_BIR_III_2 | 99 | 103 | PF00653 | 0.591 |
LIG_BRCT_BRCA1_1 | 525 | 529 | PF00533 | 0.586 |
LIG_CaM_IQ_9 | 225 | 241 | PF13499 | 0.625 |
LIG_EVH1_1 | 186 | 190 | PF00568 | 0.734 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.750 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.670 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.640 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.666 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.490 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.367 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.696 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.744 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.582 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.711 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.530 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.556 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.518 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.519 |
LIG_KLC1_Yacidic_2 | 489 | 493 | PF13176 | 0.434 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.775 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.635 |
LIG_PDZ_Class_2 | 538 | 543 | PF00595 | 0.730 |
LIG_Pex14_1 | 420 | 424 | PF04695 | 0.606 |
LIG_PTAP_UEV_1 | 303 | 308 | PF05743 | 0.712 |
LIG_SH2_CRK | 235 | 239 | PF00017 | 0.702 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.599 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.535 |
LIG_SH2_GRB2like | 11 | 14 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.569 |
LIG_SH2_STAT3 | 505 | 508 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.702 |
LIG_SH3_1 | 137 | 143 | PF00018 | 0.783 |
LIG_SH3_1 | 248 | 254 | PF00018 | 0.545 |
LIG_SH3_2 | 304 | 309 | PF14604 | 0.722 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.834 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.738 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.605 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.702 |
LIG_SUMO_SIM_anti_2 | 340 | 345 | PF11976 | 0.389 |
LIG_SUMO_SIM_anti_2 | 49 | 58 | PF11976 | 0.698 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.694 |
LIG_UBA3_1 | 264 | 273 | PF00899 | 0.587 |
LIG_UBA3_1 | 36 | 41 | PF00899 | 0.649 |
LIG_WW_3 | 139 | 143 | PF00397 | 0.549 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.740 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.645 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.514 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.620 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.757 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.643 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.535 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.714 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.530 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.490 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.513 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.750 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.703 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.601 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.618 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.753 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.555 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.647 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.800 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.698 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.694 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.609 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.713 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.476 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.581 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.413 |
MOD_LATS_1 | 485 | 491 | PF00433 | 0.530 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.600 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.502 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.433 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.609 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.541 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.498 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.811 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.779 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.565 |
MOD_PKA_1 | 203 | 209 | PF00069 | 0.779 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.715 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.396 |
MOD_PKA_1 | 527 | 533 | PF00069 | 0.617 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.641 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.779 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.779 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.645 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.540 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.703 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.535 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.542 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.689 |
MOD_PKB_1 | 439 | 447 | PF00069 | 0.599 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.641 |
MOD_Plk_2-3 | 119 | 125 | PF00069 | 0.770 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.568 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.497 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.440 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.555 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.793 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.763 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.716 |
MOD_SUMO_for_1 | 400 | 403 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 218 | 224 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 266 | 275 | PF00179 | 0.571 |
MOD_SUMO_rev_2 | 360 | 369 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 421 | 430 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 489 | 497 | PF00179 | 0.609 |
TRG_DiLeu_BaEn_1 | 52 | 57 | PF01217 | 0.696 |
TRG_DiLeu_BaLyEn_6 | 260 | 265 | PF01217 | 0.646 |
TRG_DiLeu_BaLyEn_6 | 453 | 458 | PF01217 | 0.621 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.765 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.654 |
TRG_NES_CRM1_1 | 34 | 49 | PF08389 | 0.440 |
TRG_NES_CRM1_1 | 340 | 351 | PF08389 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 109 | 113 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 363 | 367 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 456 | 460 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 514 | 518 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IKZ7 | Leishmania donovani | 89% | 100% |
A4HKC0 | Leishmania braziliensis | 68% | 100% |
A4I7U9 | Leishmania infantum | 89% | 100% |
Q4Q5F0 | Leishmania major | 87% | 100% |