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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9ADK0
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.634 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.733 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.541 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.712 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.588 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.589 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 383 | 389 | PF00134 | 0.626 |
DOC_CYCLIN_yCln2_LP_2 | 98 | 104 | PF00134 | 0.494 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.668 |
DOC_PP4_FxxP_1 | 128 | 131 | PF00568 | 0.424 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.756 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.602 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.686 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 187 | 191 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.654 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.441 |
LIG_BRCT_BRCA1_1 | 221 | 225 | PF00533 | 0.798 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.613 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.649 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.581 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.573 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.706 |
LIG_IBAR_NPY_1 | 370 | 372 | PF08397 | 0.678 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 59 | 66 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.607 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.692 |
LIG_SH2_GRB2like | 104 | 107 | PF00017 | 0.555 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.565 |
LIG_SH3_2 | 386 | 391 | PF14604 | 0.675 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.563 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.582 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.531 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.627 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.642 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.667 |
MOD_CDC14_SPxK_1 | 360 | 363 | PF00782 | 0.630 |
MOD_CDC14_SPxK_1 | 375 | 378 | PF00782 | 0.557 |
MOD_CDC14_SPxK_1 | 388 | 391 | PF00782 | 0.570 |
MOD_CDK_SPK_2 | 182 | 187 | PF00069 | 0.615 |
MOD_CDK_SPK_2 | 357 | 362 | PF00069 | 0.695 |
MOD_CDK_SPxK_1 | 136 | 142 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 357 | 363 | PF00069 | 0.631 |
MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.556 |
MOD_CDK_SPxK_1 | 385 | 391 | PF00069 | 0.571 |
MOD_CDK_SPxxK_3 | 142 | 149 | PF00069 | 0.590 |
MOD_CDK_SPxxK_3 | 169 | 176 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 6 | 13 | PF00069 | 0.621 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.612 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.627 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.480 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.649 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.651 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.611 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.589 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.682 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.673 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.633 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.630 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.677 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.674 |
MOD_DYRK1A_RPxSP_1 | 142 | 146 | PF00069 | 0.615 |
MOD_DYRK1A_RPxSP_1 | 149 | 153 | PF00069 | 0.529 |
MOD_DYRK1A_RPxSP_1 | 301 | 305 | PF00069 | 0.686 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.684 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.732 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.796 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.471 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.616 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.803 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.669 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.635 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.594 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.632 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.725 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.534 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.639 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.596 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.598 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.587 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.618 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.647 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.587 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.655 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.701 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.541 |
MOD_LATS_1 | 174 | 180 | PF00433 | 0.585 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.620 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.645 |
MOD_N-GLC_2 | 110 | 112 | PF02516 | 0.410 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.684 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.637 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.670 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.641 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.605 |
MOD_OFUCOSY | 120 | 126 | PF10250 | 0.420 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.565 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.632 |
MOD_PK_1 | 176 | 182 | PF00069 | 0.576 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.435 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.620 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.607 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.607 |
MOD_PKB_1 | 142 | 150 | PF00069 | 0.616 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.501 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.622 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.604 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.586 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.579 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.596 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.721 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.605 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.461 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.532 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.606 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.690 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.698 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.533 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.630 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.539 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.634 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.651 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.609 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.634 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W6 | Leptomonas seymouri | 41% | 100% |
A0A3S7X1G7 | Leishmania donovani | 95% | 100% |
A4HGJ2 | Leishmania braziliensis | 68% | 100% |
E9AHG4 | Leishmania infantum | 95% | 100% |
E9AZW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |